Run ID: ERR216965
Sample name:
Date: 31-03-2023 15:57:08
Number of reads: 46649
Percentage reads mapped: 4.37
Strain: lineage4.9
Drug-resistance: HR-TB
| Drug | Resistance | Supporting mutations |
|---|
| Lineage | Family | Main Spoligotype | RDs | Frequency |
|---|---|---|---|---|
| lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
| lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
| Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
|---|---|---|---|---|---|
| gyrA | 7572 | p.Ser91Ala | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
| katG | 2155693 | p.Ser140Asn | missense_variant | 1.0 | isoniazid |
| Gene | Chromosome position | Mutation | Type | Estimated fraction |
|---|---|---|---|---|
| gyrB | 6079 | c.840C>T | synonymous_variant | 1.0 |
| gyrB | 6098 | p.Val287Leu | missense_variant | 1.0 |
| gyrB | 6104 | p.Ile289Val | missense_variant | 1.0 |
| gyrB | 6109 | c.870G>C | synonymous_variant | 1.0 |
| gyrB | 6115 | c.876A>G | synonymous_variant | 1.0 |
| gyrB | 6122 | p.Ala295Ser | missense_variant | 1.0 |
| gyrB | 6127 | c.888G>A | synonymous_variant | 1.0 |
| gyrB | 6130 | c.891T>C | synonymous_variant | 1.0 |
| gyrB | 6133 | c.894G>C | synonymous_variant | 1.0 |
| gyrB | 6181 | c.942C>T | synonymous_variant | 1.0 |
| gyrB | 6184 | c.945C>G | synonymous_variant | 1.0 |
| gyrA | 6484 | c.-818A>G | upstream_gene_variant | 0.6 |
| gyrA | 6490 | c.-812T>G | upstream_gene_variant | 0.6 |
| gyrB | 6491 | p.Ile418Val | missense_variant | 0.6 |
| gyrA | 6496 | c.-806G>C | upstream_gene_variant | 0.6 |
| gyrA | 6499 | c.-803A>C | upstream_gene_variant | 0.6 |
| gyrA | 6508 | c.-794A>G | upstream_gene_variant | 0.8 |
| gyrA | 6511 | c.-791A>C | upstream_gene_variant | 0.8 |
| gyrA | 6515 | c.-787T>C | upstream_gene_variant | 0.8 |
| gyrA | 6520 | c.-782G>C | upstream_gene_variant | 0.8 |
| gyrA | 6526 | c.-776T>C | upstream_gene_variant | 0.8 |
| gyrA | 6535 | c.-767C>G | upstream_gene_variant | 0.8 |
| gyrA | 6541 | c.-761C>T | upstream_gene_variant | 0.8 |
| gyrA | 6550 | c.-752A>T | upstream_gene_variant | 0.8 |
| gyrA | 6551 | c.-751T>C | upstream_gene_variant | 1.0 |
| gyrA | 6745 | c.-557T>C | upstream_gene_variant | 1.0 |
| gyrB | 6749 | p.Ala504Ser | missense_variant | 1.0 |
| gyrA | 6760 | c.-542G>C | upstream_gene_variant | 1.0 |
| gyrB | 6764 | p.Leu509Phe | missense_variant | 1.0 |
| gyrA | 6775 | c.-527G>T | upstream_gene_variant | 1.0 |
| gyrA | 6793 | c.-509T>C | upstream_gene_variant | 1.0 |
| gyrB | 6794 | p.Ile519Leu | missense_variant | 1.0 |
| gyrB | 6797 | p.Gly520Ser | missense_variant | 1.0 |
| gyrA | 6802 | c.-500G>A | upstream_gene_variant | 1.0 |
| gyrA | 6823 | c.-479G>C | upstream_gene_variant | 1.0 |
| gyrA | 6835 | c.-467C>T | upstream_gene_variant | 1.0 |
| gyrA | 6841 | c.-461T>C | upstream_gene_variant | 1.0 |
| gyrA | 6844 | c.-458T>G | upstream_gene_variant | 1.0 |
| gyrA | 6853 | c.-449A>G | upstream_gene_variant | 1.0 |
| gyrA | 6865 | c.-437G>C | upstream_gene_variant | 1.0 |
| gyrA | 6869 | c.-433T>C | upstream_gene_variant | 1.0 |
| gyrA | 6872 | c.-430T>C | upstream_gene_variant | 1.0 |
| gyrA | 6877 | c.-425G>C | upstream_gene_variant | 1.0 |
| gyrA | 6878 | c.-424T>C | upstream_gene_variant | 1.0 |
| gyrA | 6881 | c.-421T>C | upstream_gene_variant | 1.0 |
| gyrA | 6898 | c.-404G>C | upstream_gene_variant | 1.0 |
| gyrA | 7569 | p.Ala90Ser | missense_variant | 1.0 |
| gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
| gyrA | 7592 | c.291G>C | synonymous_variant | 1.0 |
| gyrA | 7595 | c.294C>G | synonymous_variant | 1.0 |
| gyrA | 7611 | p.Ser104Ala | missense_variant | 1.0 |
| gyrA | 7614 | p.Leu105Met | missense_variant | 1.0 |
| gyrA | 7619 | c.318C>G | synonymous_variant | 1.0 |
| gyrA | 7631 | c.330G>C | synonymous_variant | 1.0 |
| gyrA | 8288 | c.987T>C | synonymous_variant | 1.0 |
| gyrA | 8294 | c.993T>C | synonymous_variant | 1.0 |
| gyrA | 8321 | c.1020C>T | synonymous_variant | 1.0 |
| gyrA | 8324 | c.1023T>C | synonymous_variant | 1.0 |
| gyrA | 8330 | c.1029C>G | synonymous_variant | 1.0 |
| gyrA | 8333 | c.1032C>T | synonymous_variant | 1.0 |
| gyrA | 8339 | c.1038A>C | synonymous_variant | 1.0 |
| gyrA | 8340 | p.Ala347Ser | missense_variant | 1.0 |
| gyrA | 8351 | p.Asp350Glu | missense_variant | 1.0 |
| gyrA | 8354 | c.1053G>T | synonymous_variant | 1.0 |
| gyrA | 8363 | c.1062C>T | synonymous_variant | 1.0 |
| gyrA | 8366 | c.1065G>C | synonymous_variant | 1.0 |
| gyrA | 8378 | c.1077C>T | synonymous_variant | 1.0 |
| gyrA | 8382 | p.Leu361Met | missense_variant | 1.0 |
| gyrA | 8829 | c.1528T>C | synonymous_variant | 0.75 |
| gyrA | 8849 | c.1548C>G | synonymous_variant | 0.89 |
| gyrA | 8852 | c.1551T>G | synonymous_variant | 0.89 |
| gyrA | 8858 | c.1557T>G | synonymous_variant | 0.89 |
| gyrA | 8861 | c.1560C>T | synonymous_variant | 0.89 |
| gyrA | 8867 | c.1566A>G | synonymous_variant | 0.89 |
| gyrA | 8870 | c.1569G>C | synonymous_variant | 0.89 |
| gyrA | 8873 | c.1572A>T | synonymous_variant | 0.9 |
| gyrA | 8876 | c.1575C>T | synonymous_variant | 0.91 |
| gyrA | 8900 | c.1599G>C | synonymous_variant | 0.94 |
| gyrA | 8903 | c.1602T>C | synonymous_variant | 0.94 |
| gyrA | 8921 | c.1620C>T | synonymous_variant | 0.87 |
| gyrA | 8924 | c.1623C>T | synonymous_variant | 0.93 |
| gyrA | 8930 | c.1629C>T | synonymous_variant | 0.92 |
| gyrA | 8942 | c.1641G>C | synonymous_variant | 0.88 |
| gyrA | 8960 | c.1659C>T | synonymous_variant | 0.88 |
| gyrA | 8967 | p.Ala556Lys | missense_variant | 0.8 |
| fgd1 | 491112 | c.330G>A | synonymous_variant | 1.0 |
| fgd1 | 491121 | c.339A>G | synonymous_variant | 1.0 |
| fgd1 | 491138 | p.Glu119Ala | missense_variant | 1.0 |
| fgd1 | 491144 | p.Ala121Glu | missense_variant | 1.0 |
| fgd1 | 491166 | c.384G>A | synonymous_variant | 1.0 |
| fgd1 | 491172 | c.390C>G | synonymous_variant | 1.0 |
| fgd1 | 491175 | c.393G>C | synonymous_variant | 1.0 |
| fgd1 | 491181 | c.399T>G | synonymous_variant | 1.0 |
| rpoB | 760148 | p.Asp114Glu | missense_variant | 1.0 |
| rpoB | 760157 | c.351A>G | synonymous_variant | 1.0 |
| rpoB | 760166 | c.360C>T | synonymous_variant | 1.0 |
| rpoB | 760172 | c.366G>C | synonymous_variant | 1.0 |
| rpoB | 760181 | c.375T>G | synonymous_variant | 1.0 |
| rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
| rpoB | 760185 | c.379C>T | synonymous_variant | 1.0 |
| rpoB | 760199 | c.393C>G | synonymous_variant | 1.0 |
| rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
| rpoB | 760256 | c.450C>T | synonymous_variant | 1.0 |
| rpoB | 760262 | c.456G>C | synonymous_variant | 1.0 |
| rpoB | 760274 | p.Glu156Asp | missense_variant | 1.0 |
| rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
| rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
| rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
| rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
| rpoB | 760317 | c.511_513delAGCinsTCT | synonymous_variant | 1.0 |
| rpoB | 760331 | c.525G>T | synonymous_variant | 1.0 |
| rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
| rpoB | 760427 | c.621G>A | synonymous_variant | 1.0 |
| rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
| rpoB | 760433 | c.627C>T | synonymous_variant | 1.0 |
| rpoB | 760457 | c.651C>T | synonymous_variant | 1.0 |
| rpoB | 760463 | c.657C>G | synonymous_variant | 1.0 |
| rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
| rpoB | 760481 | c.675G>T | synonymous_variant | 1.0 |
| rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
| rpoB | 760490 | c.684C>G | synonymous_variant | 1.0 |
| rpoB | 760496 | c.690G>T | synonymous_variant | 1.0 |
| rpoB | 760508 | c.702G>C | synonymous_variant | 1.0 |
| rpoB | 760511 | c.705G>C | synonymous_variant | 1.0 |
| rpoB | 760628 | c.822G>A | synonymous_variant | 1.0 |
| rpoB | 760643 | c.837G>A | synonymous_variant | 1.0 |
| rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
| rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
| rpoB | 760658 | c.852G>A | synonymous_variant | 1.0 |
| rpoB | 760659 | p.Ser285Ala | missense_variant | 1.0 |
| rpoB | 760670 | c.864G>C | synonymous_variant | 1.0 |
| rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
| rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
| rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
| rpoB | 760868 | c.1062C>G | synonymous_variant | 1.0 |
| rpoB | 760877 | c.1071G>A | synonymous_variant | 1.0 |
| rpoB | 760886 | c.1080A>G | synonymous_variant | 1.0 |
| rpoB | 760887 | p.Thr361Val | missense_variant | 1.0 |
| rpoB | 760895 | c.1089C>T | synonymous_variant | 1.0 |
| rpoB | 760916 | c.1110C>T | synonymous_variant | 1.0 |
| rpoB | 760919 | c.1113C>T | synonymous_variant | 1.0 |
| rpoB | 760920 | p.Leu372Ile | missense_variant | 1.0 |
| rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
| rpoB | 760934 | c.1128C>T | synonymous_variant | 1.0 |
| rpoB | 760937 | c.1131G>A | synonymous_variant | 1.0 |
| rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
| rpoB | 760958 | c.1152G>C | synonymous_variant | 1.0 |
| rpoB | 760991 | c.1185G>T | synonymous_variant | 1.0 |
| rpoB | 760997 | c.1191G>C | synonymous_variant | 1.0 |
| rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
| rpoB | 761027 | c.1221A>C | synonymous_variant | 1.0 |
| rpoB | 761036 | c.1230G>C | synonymous_variant | 1.0 |
| rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
| rpoB | 761051 | c.1245G>C | synonymous_variant | 1.0 |
| rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
| rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
| rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
| rpoB | 761063 | c.1257C>G | synonymous_variant | 1.0 |
| rpoB | 761088 | c.1282_1284delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 1.0 |
| rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
| rpoB | 761132 | c.1326G>C | synonymous_variant | 1.0 |
| rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
| rpoB | 761150 | c.1344A>T | synonymous_variant | 1.0 |
| rpoB | 761154 | p.Ser450Asn | missense_variant | 1.0 |
| rpoB | 761165 | c.1359G>C | synonymous_variant | 1.0 |
| rpoB | 761171 | c.1365C>T | synonymous_variant | 1.0 |
| rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
| rpoB | 761189 | c.1383T>G | synonymous_variant | 1.0 |
| rpoB | 761195 | c.1389G>T | synonymous_variant | 1.0 |
| rpoB | 761201 | c.1395G>A | synonymous_variant | 1.0 |
| rpoB | 761204 | c.1398C>G | synonymous_variant | 1.0 |
| rpoB | 761255 | c.1449T>G | synonymous_variant | 1.0 |
| rpoB | 761258 | c.1452G>A | synonymous_variant | 1.0 |
| rpoB | 761261 | c.1455G>C | synonymous_variant | 1.0 |
| rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
| rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
| rpoB | 761282 | c.1476C>T | synonymous_variant | 1.0 |
| rpoB | 761289 | p.Ser495Ala | missense_variant | 1.0 |
| rpoB | 761537 | c.1731C>G | synonymous_variant | 1.0 |
| rpoB | 761561 | c.1755C>G | synonymous_variant | 1.0 |
| rpoB | 761564 | c.1758G>C | synonymous_variant | 1.0 |
| rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
| rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
| rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
| rpoB | 761612 | c.1806G>C | synonymous_variant | 1.0 |
| rpoB | 761615 | c.1809A>G | synonymous_variant | 1.0 |
| rpoB | 761627 | c.1821C>T | synonymous_variant | 1.0 |
| rpoB | 761633 | c.1827G>C | synonymous_variant | 1.0 |
| rpoB | 761948 | c.2142G>C | synonymous_variant | 1.0 |
| rpoB | 761954 | c.2148C>G | synonymous_variant | 1.0 |
| rpoB | 761972 | c.2166C>T | synonymous_variant | 1.0 |
| rpoB | 762002 | c.2196C>G | synonymous_variant | 1.0 |
| rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
| rpoB | 762011 | c.2205G>C | synonymous_variant | 1.0 |
| rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
| rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
| rpoB | 762020 | p.Glu738Asp | missense_variant | 1.0 |
| rpoB | 762026 | c.2220G>T | synonymous_variant | 1.0 |
| rpoB | 762041 | c.2235C>T | synonymous_variant | 1.0 |
| rpoB | 762047 | c.2241G>A | synonymous_variant | 1.0 |
| rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
| rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
| rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
| rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
| rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
| rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
| rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
| rpoB | 762137 | c.2331C>T | synonymous_variant | 1.0 |
| rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
| rpoB | 762161 | c.2355C>T | synonymous_variant | 1.0 |
| rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
| rpoB | 762170 | c.2364C>G | synonymous_variant | 1.0 |
| rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
| rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
| rpoB | 762188 | c.2382C>T | synonymous_variant | 1.0 |
| rpoB | 762206 | c.2400C>G | synonymous_variant | 1.0 |
| rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
| rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
| rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
| rpoB | 762290 | c.2484C>T | synonymous_variant | 1.0 |
| rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
| rpoB | 762314 | c.2508C>T | synonymous_variant | 1.0 |
| rpoC | 762830 | c.-540C>T | upstream_gene_variant | 1.0 |
| rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 1.0 |
| rpoC | 762839 | c.-531G>A | upstream_gene_variant | 1.0 |
| rpoC | 762848 | c.-522G>C | upstream_gene_variant | 1.0 |
| rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
| rpoB | 762858 | p.Thr1018Ala | missense_variant | 1.0 |
| rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
| rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
| rpoC | 762896 | c.-474G>C | upstream_gene_variant | 1.0 |
| rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
| rpoC | 762923 | c.-447C>G | upstream_gene_variant | 1.0 |
| rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
| rpoC | 762959 | c.-411G>C | upstream_gene_variant | 1.0 |
| rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
| rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
| rpoC | 762989 | c.-381G>T | upstream_gene_variant | 1.0 |
| rpoC | 762995 | c.-375G>C | upstream_gene_variant | 1.0 |
| rpoC | 762998 | c.-372G>A | upstream_gene_variant | 1.0 |
| rpoC | 763004 | c.-366G>A | upstream_gene_variant | 1.0 |
| rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
| rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
| rpoC | 763049 | c.-321G>A | upstream_gene_variant | 1.0 |
| rpoC | 763053 | c.-317T>C | upstream_gene_variant | 1.0 |
| rpoB | 763074 | p.Thr1090Val | missense_variant | 1.0 |
| rpoC | 763079 | c.-291C>G | upstream_gene_variant | 1.0 |
| rpoC | 763085 | c.-285C>G | upstream_gene_variant | 1.0 |
| rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
| rpoC | 763103 | c.-267G>C | upstream_gene_variant | 1.0 |
| rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
| rpoC | 763124 | c.-246C>T | upstream_gene_variant | 1.0 |
| rpoC | 763139 | c.-231C>T | upstream_gene_variant | 1.0 |
| rpoC | 763142 | c.-228C>G | upstream_gene_variant | 1.0 |
| rpoC | 763145 | c.-225G>A | upstream_gene_variant | 1.0 |
| rpoC | 763157 | c.-213G>T | upstream_gene_variant | 1.0 |
| rpoC | 763163 | c.-207C>G | upstream_gene_variant | 1.0 |
| rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
| rpoC | 763172 | c.-198G>C | upstream_gene_variant | 1.0 |
| rpoC | 763190 | c.-180C>T | upstream_gene_variant | 1.0 |
| rpoC | 763193 | c.-177C>G | upstream_gene_variant | 1.0 |
| rpoC | 763363 | c.-7G>A | upstream_gene_variant | 1.0 |
| rpoC | 763375 | c.6C>A | synonymous_variant | 1.0 |
| rpoC | 763402 | c.33C>G | synonymous_variant | 1.0 |
| rpoC | 763408 | c.39T>C | synonymous_variant | 1.0 |
| rpoC | 763411 | c.42T>G | synonymous_variant | 1.0 |
| rpoC | 763414 | c.45T>C | synonymous_variant | 1.0 |
| rpoC | 763420 | c.51G>C | synonymous_variant | 1.0 |
| rpoC | 763423 | p.Glu18Asp | missense_variant | 1.0 |
| rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 1.0 |
| rpoC | 763435 | c.66A>G | synonymous_variant | 1.0 |
| rpoC | 763444 | c.75T>C | synonymous_variant | 1.0 |
| rpoC | 763453 | c.84C>G | synonymous_variant | 1.0 |
| rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
| rpoC | 763459 | c.90G>A | synonymous_variant | 1.0 |
| rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
| rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
| rpoC | 763528 | c.159G>C | synonymous_variant | 1.0 |
| rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
| rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
| rpoC | 763537 | c.168C>G | synonymous_variant | 1.0 |
| rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
| rpoC | 763558 | c.189C>T | synonymous_variant | 1.0 |
| rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
| rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
| rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
| rpoC | 763597 | c.228G>A | synonymous_variant | 1.0 |
| rpoC | 763624 | c.255C>G | synonymous_variant | 1.0 |
| rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
| rpoC | 763651 | c.282C>T | synonymous_variant | 1.0 |
| rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
| rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
| rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
| rpoC | 763747 | c.378G>A | synonymous_variant | 1.0 |
| rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
| rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
| rpoC | 763781 | c.412_414delTCGinsAGC | synonymous_variant | 1.0 |
| rpoC | 763801 | c.432C>G | synonymous_variant | 1.0 |
| rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
| rpoC | 764032 | p.Asp221Glu | missense_variant | 1.0 |
| rpoC | 764040 | p.Ser224Asn | missense_variant | 1.0 |
| rpoC | 764044 | c.675T>C | synonymous_variant | 1.0 |
| rpoC | 764059 | c.690G>C | synonymous_variant | 1.0 |
| rpoC | 764077 | c.708C>G | synonymous_variant | 1.0 |
| rpoC | 764083 | c.714A>G | synonymous_variant | 1.0 |
| rpoC | 764084 | p.Asn239Ala | missense_variant | 1.0 |
| rpoC | 764098 | c.729A>G | synonymous_variant | 1.0 |
| rpoC | 764102 | p.Val245Thr | missense_variant | 1.0 |
| rpoC | 764131 | c.762T>C | synonymous_variant | 1.0 |
| rpoC | 764134 | c.765C>G | synonymous_variant | 0.86 |
| rpoC | 764149 | c.780G>C | synonymous_variant | 1.0 |
| rpoC | 764320 | c.951C>A | synonymous_variant | 1.0 |
| rpoC | 764344 | c.975C>G | synonymous_variant | 1.0 |
| rpoC | 764353 | c.984G>C | synonymous_variant | 1.0 |
| rpoC | 764365 | c.996C>T | synonymous_variant | 1.0 |
| rpoC | 764371 | c.1002G>T | synonymous_variant | 1.0 |
| rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
| rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
| rpoC | 764395 | c.1026C>T | synonymous_variant | 1.0 |
| rpoC | 764398 | c.1029G>C | synonymous_variant | 1.0 |
| rpoC | 764405 | c.1036A>C | synonymous_variant | 1.0 |
| rpoC | 764410 | c.1041G>C | synonymous_variant | 1.0 |
| rpoC | 764428 | c.1059G>C | synonymous_variant | 1.0 |
| rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
| rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
| rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 1.0 |
| rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
| rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
| rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
| rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
| rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
| rpoC | 764500 | c.1131C>G | synonymous_variant | 1.0 |
| rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
| rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
| rpoC | 764548 | c.1179G>C | synonymous_variant | 1.0 |
| rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
| rpoC | 764566 | c.1197C>G | synonymous_variant | 1.0 |
| rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
| rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
| rpoC | 764593 | c.1224C>T | synonymous_variant | 1.0 |
| rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
| rpoC | 764644 | c.1275G>C | synonymous_variant | 1.0 |
| rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
| rpoC | 764662 | c.1293G>C | synonymous_variant | 1.0 |
| rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
| rpoC | 764680 | c.1311G>A | synonymous_variant | 1.0 |
| rpoC | 764686 | c.1317C>T | synonymous_variant | 1.0 |
| rpoC | 764692 | c.1323C>T | synonymous_variant | 1.0 |
| rpoC | 764705 | c.1336C>T | synonymous_variant | 1.0 |
| rpoC | 764731 | c.1362G>C | synonymous_variant | 1.0 |
| rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
| rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
| rpoC | 764779 | c.1410G>A | synonymous_variant | 1.0 |
| rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 1.0 |
| rpoC | 764791 | c.1422C>G | synonymous_variant | 1.0 |
| rpoC | 764803 | c.1434C>G | synonymous_variant | 1.0 |
| rpoC | 764809 | c.1440C>G | synonymous_variant | 1.0 |
| rpoC | 764812 | c.1443C>A | synonymous_variant | 1.0 |
| rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
| rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
| rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
| rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
| rpoC | 764863 | c.1494G>C | synonymous_variant | 1.0 |
| rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
| rpoC | 764872 | c.1503A>G | synonymous_variant | 1.0 |
| rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
| rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
| rpoC | 764912 | p.Met515Gln | missense_variant | 1.0 |
| rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
| rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
| rpoC | 764939 | c.1570C>T | synonymous_variant | 1.0 |
| rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
| rpoC | 764953 | c.1584G>C | synonymous_variant | 1.0 |
| rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
| rpoC | 765757 | c.2388C>T | synonymous_variant | 1.0 |
| rpoC | 765772 | c.2403C>G | synonymous_variant | 1.0 |
| rpoC | 765781 | c.2412C>T | synonymous_variant | 1.0 |
| rpoC | 765784 | c.2415C>G | synonymous_variant | 1.0 |
| rpoC | 765793 | c.2424C>G | synonymous_variant | 1.0 |
| rpoC | 765796 | c.2427C>T | synonymous_variant | 1.0 |
| rpoC | 765811 | c.2442T>C | synonymous_variant | 1.0 |
| rpoC | 765814 | c.2445A>T | synonymous_variant | 1.0 |
| rpoC | 765817 | c.2448G>C | synonymous_variant | 1.0 |
| rpoC | 765820 | c.2451G>C | synonymous_variant | 1.0 |
| rpoC | 765844 | c.2475C>G | synonymous_variant | 1.0 |
| rpoC | 765871 | c.2502T>G | synonymous_variant | 1.0 |
| rpoC | 765875 | p.Val836Ile | missense_variant | 1.0 |
| rpoC | 765886 | c.2517C>G | synonymous_variant | 1.0 |
| rpoC | 765904 | c.2535C>G | synonymous_variant | 1.0 |
| rpoC | 765907 | c.2538G>T | synonymous_variant | 1.0 |
| rpoC | 765937 | c.2568T>G | synonymous_variant | 1.0 |
| rpoC | 765940 | c.2571A>T | synonymous_variant | 1.0 |
| rpoC | 765946 | c.2577C>T | synonymous_variant | 1.0 |
| rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
| rpoC | 765952 | c.2583G>C | synonymous_variant | 1.0 |
| rpoC | 765955 | c.2586C>T | synonymous_variant | 1.0 |
| rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
| rpoC | 765979 | c.2610C>G | synonymous_variant | 1.0 |
| rpoC | 765982 | c.2613C>T | synonymous_variant | 1.0 |
| rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
| rpoC | 766012 | c.2643C>G | synonymous_variant | 1.0 |
| rpoC | 766030 | c.2661C>G | synonymous_variant | 1.0 |
| rpoC | 766034 | p.His889Thr | missense_variant | 1.0 |
| rpoC | 766043 | p.Gln892Gly | missense_variant | 1.0 |
| rpoC | 766390 | c.3021C>T | synonymous_variant | 1.0 |
| rpoC | 766408 | c.3039C>T | synonymous_variant | 1.0 |
| rpoC | 766411 | c.3042C>G | synonymous_variant | 1.0 |
| rpoC | 766425 | c.3056_3057insTGT | disruptive_inframe_insertion | 1.0 |
| rpoC | 766428 | p.Val1020Ala | missense_variant | 1.0 |
| rpoC | 766435 | p.Glu1022Asp | missense_variant | 1.0 |
| rpoC | 766456 | c.3087C>G | synonymous_variant | 1.0 |
| rpoC | 766459 | c.3090G>T | synonymous_variant | 1.0 |
| rpoC | 766471 | c.3102G>C | synonymous_variant | 1.0 |
| rpoC | 766703 | p.Met1112Leu | missense_variant | 1.0 |
| rpoC | 766708 | c.3339A>G | synonymous_variant | 1.0 |
| rpoC | 766712 | p.Ser1115Ala | missense_variant | 1.0 |
| rpoC | 766717 | c.3348C>G | synonymous_variant | 1.0 |
| rpoC | 766753 | c.3384C>G | synonymous_variant | 1.0 |
| rpoC | 766754 | p.Glu1129Gln | missense_variant | 1.0 |
| rpoC | 766759 | c.3390G>A | synonymous_variant | 1.0 |
| rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
| rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
| rpoC | 766776 | p.Arg1136His | missense_variant | 1.0 |
| rpoC | 766798 | c.3429C>G | synonymous_variant | 1.0 |
| rpoC | 766799 | p.Ala1144Ser | missense_variant | 1.0 |
| rpoC | 766804 | c.3435A>G | synonymous_variant | 1.0 |
| rpoC | 766813 | c.3444G>C | synonymous_variant | 1.0 |
| rpoC | 766837 | c.3468G>C | synonymous_variant | 1.0 |
| rpoC | 766843 | c.3474T>C | synonymous_variant | 1.0 |
| rpoC | 767167 | c.3798C>G | synonymous_variant | 1.0 |
| rpoC | 767180 | p.Ala1271Gln | missense_variant | 1.0 |
| rpoC | 767185 | c.3816G>T | synonymous_variant | 1.0 |
| rpoC | 767191 | c.3822C>G | synonymous_variant | 1.0 |
| rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
| rpsL | 781682 | c.123T>C | synonymous_variant | 1.0 |
| rpsL | 781700 | c.141G>C | synonymous_variant | 1.0 |
| rpsL | 781706 | c.147T>G | synonymous_variant | 1.0 |
| rpsL | 781715 | c.156T>C | synonymous_variant | 1.0 |
| rpsL | 781718 | c.159C>G | synonymous_variant | 1.0 |
| rpsL | 781721 | c.162C>T | synonymous_variant | 1.0 |
| rpsL | 781728 | c.169T>C | synonymous_variant | 1.0 |
| rpsL | 781733 | c.174G>C | synonymous_variant | 1.0 |
| rpsL | 781736 | c.177T>C | synonymous_variant | 1.0 |
| rpsL | 781737 | p.Gln60Ala | missense_variant | 1.0 |
| rpsL | 781754 | c.195G>C | synonymous_variant | 1.0 |
| rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
| rpsL | 781766 | c.207C>T | synonymous_variant | 1.0 |
| rpsL | 781769 | c.210G>A | synonymous_variant | 1.0 |
| rpsL | 781772 | c.213C>G | synonymous_variant | 1.0 |
| rpsL | 781793 | c.234G>C | synonymous_variant | 1.0 |
| rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
| rpsL | 781805 | c.246G>T | synonymous_variant | 1.0 |
| rpsL | 781814 | c.255C>T | synonymous_variant | 1.0 |
| rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
| rpsL | 781823 | c.264G>A | synonymous_variant | 1.0 |
| rpsL | 781829 | c.270G>C | synonymous_variant | 1.0 |
| rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
| rpsL | 781841 | c.282C>T | synonymous_variant | 1.0 |
| rpsL | 781898 | c.339A>C | synonymous_variant | 1.0 |
| rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
| rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
| rplC | 800645 | c.-164C>T | upstream_gene_variant | 1.0 |
| rplC | 800648 | c.-161A>G | upstream_gene_variant | 1.0 |
| rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
| rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
| rplC | 800690 | c.-119C>T | upstream_gene_variant | 1.0 |
| rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
| rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
| rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
| rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
| rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
| rplC | 800735 | c.-74C>G | upstream_gene_variant | 1.0 |
| rplC | 800738 | c.-71T>G | upstream_gene_variant | 1.0 |
| rplC | 800762 | c.-47T>G | upstream_gene_variant | 1.0 |
| rplC | 801171 | c.363A>G | synonymous_variant | 1.0 |
| rplC | 801195 | c.387G>T | synonymous_variant | 1.0 |
| rplC | 801207 | c.399C>T | synonymous_variant | 1.0 |
| rplC | 801220 | c.412_414delAGTinsTCC | synonymous_variant | 1.0 |
| rplC | 801231 | c.423C>G | synonymous_variant | 1.0 |
| rplC | 801237 | c.429G>C | synonymous_variant | 1.0 |
| rplC | 801246 | c.438C>T | synonymous_variant | 1.0 |
| rplC | 801249 | c.441T>C | synonymous_variant | 1.0 |
| rplC | 801255 | c.447C>T | synonymous_variant | 1.0 |
| fbiC | 1304559 | p.Glu543Asp | missense_variant | 1.0 |
| fbiC | 1304562 | c.1632G>C | synonymous_variant | 1.0 |
| fbiC | 1304567 | p.Phe546Tyr | missense_variant | 1.0 |
| fbiC | 1304574 | c.1644C>G | synonymous_variant | 1.0 |
| fbiC | 1304580 | c.1650T>C | synonymous_variant | 1.0 |
| fbiC | 1304583 | c.1653C>T | synonymous_variant | 1.0 |
| fbiC | 1304598 | c.1668C>T | synonymous_variant | 1.0 |
| fbiC | 1304619 | c.1689G>T | synonymous_variant | 1.0 |
| fbiC | 1304634 | c.1704C>T | synonymous_variant | 1.0 |
| fbiC | 1304640 | c.1710A>C | synonymous_variant | 1.0 |
| fbiC | 1304691 | c.1761G>T | synonymous_variant | 1.0 |
| fbiC | 1304694 | c.1764A>C | synonymous_variant | 1.0 |
| fbiC | 1304703 | c.1773C>G | synonymous_variant | 1.0 |
| fbiC | 1304704 | p.His592Tyr | missense_variant | 1.0 |
| fbiC | 1304709 | c.1779C>G | synonymous_variant | 1.0 |
| fbiC | 1304711 | p.Ala594Asp | missense_variant | 1.0 |
| fbiC | 1304715 | c.1785G>C | synonymous_variant | 1.0 |
| fbiC | 1304718 | c.1788C>G | synonymous_variant | 1.0 |
| fbiC | 1304724 | c.1794A>G | synonymous_variant | 1.0 |
| fbiC | 1304727 | c.1797A>C | synonymous_variant | 1.0 |
| fbiC | 1304748 | c.1818T>C | synonymous_variant | 1.0 |
| fbiC | 1304754 | p.Glu608Asp | missense_variant | 1.0 |
| fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
| rrs | 1471914 | n.69A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471943 | n.98T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471978 | n.133C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472070 | n.225G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472326 | n.481T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472328 | n.483G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472425 | n.580T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472437 | n.592T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472467 | n.622G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472486 | n.641A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.96 |
| rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.92 |
| rrs | 1472844 | n.999C>A | non_coding_transcript_exon_variant | 0.75 |
| rrs | 1472845 | n.1000G>A | non_coding_transcript_exon_variant | 0.75 |
| rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.75 |
| rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.75 |
| rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.75 |
| rrs | 1472855 | n.1011_1012insGT | non_coding_transcript_exon_variant | 0.75 |
| rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.99 |
| rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.95 |
| rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 1.0 |
| rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.98 |
| rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473768 | n.111A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1473933 | n.276_277insAG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474112 | n.455T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474294 | n.638_646delCTCTCCGGA | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474310 | n.655dupG | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474406 | n.749T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474444 | n.787G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474638 | n.981C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474664 | n.1007G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474666 | n.1009T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474670 | n.1013C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474679 | n.1022G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474684 | n.1027T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474687 | n.1030C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474711 | n.1054G>T | non_coding_transcript_exon_variant | 0.96 |
| rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.98 |
| rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475406 | n.1749T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475422 | n.1765A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475555 | n.1898T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475735 | n.2078T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476025 | n.2368G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476043 | n.2387_2388delTG | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476048 | n.2391G>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476050 | n.2394_2395insTG | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.99 |
| rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 1.0 |
| rrl | 1476683 | n.3026T>C | non_coding_transcript_exon_variant | 1.0 |
| rpsA | 1833646 | c.105T>C | synonymous_variant | 1.0 |
| rpsA | 1833652 | c.111C>T | synonymous_variant | 1.0 |
| rpsA | 1833664 | c.123C>A | synonymous_variant | 1.0 |
| rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
| rpsA | 1833685 | c.144G>C | synonymous_variant | 1.0 |
| rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
| rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
| rpsA | 1833709 | c.168C>T | synonymous_variant | 1.0 |
| rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
| rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
| rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
| rpsA | 1833754 | c.213G>A | synonymous_variant | 1.0 |
| rpsA | 1833757 | c.216C>T | synonymous_variant | 1.0 |
| rpsA | 1833760 | c.219C>T | synonymous_variant | 1.0 |
| rpsA | 1833769 | c.228C>G | synonymous_variant | 1.0 |
| rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
| rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
| rpsA | 1833793 | c.252C>T | synonymous_variant | 1.0 |
| rpsA | 1833799 | c.258C>G | synonymous_variant | 1.0 |
| rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
| rpsA | 1833811 | c.270G>C | synonymous_variant | 1.0 |
| rpsA | 1833835 | c.294C>T | synonymous_variant | 1.0 |
| rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
| rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
| rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
| rpsA | 1833859 | c.318C>G | synonymous_variant | 1.0 |
| rpsA | 1833871 | c.330G>A | synonymous_variant | 1.0 |
| rpsA | 1833874 | c.333T>C | synonymous_variant | 0.91 |
| rpsA | 1833886 | c.345C>G | synonymous_variant | 1.0 |
| rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
| rpsA | 1833919 | c.378C>T | synonymous_variant | 1.0 |
| rpsA | 1833920 | p.Lys127Arg | missense_variant | 1.0 |
| rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
| rpsA | 1833931 | c.390C>G | synonymous_variant | 1.0 |
| rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
| rpsA | 1833952 | c.411C>T | synonymous_variant | 1.0 |
| rpsA | 1833970 | c.429G>T | synonymous_variant | 1.0 |
| rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
| rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
| rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
| rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
| rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
| rpsA | 1834033 | c.492C>T | synonymous_variant | 1.0 |
| rpsA | 1834034 | p.Ile165Val | missense_variant | 0.9 |
| rpsA | 1834093 | c.552G>C | synonymous_variant | 1.0 |
| rpsA | 1834102 | c.561T>C | synonymous_variant | 1.0 |
| rpsA | 1834105 | c.564C>T | synonymous_variant | 1.0 |
| rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
| rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
| rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
| rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
| rpsA | 1834249 | c.708T>C | synonymous_variant | 0.93 |
| rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
| rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
| rpsA | 1834279 | c.738C>T | synonymous_variant | 1.0 |
| rpsA | 1834298 | p.Gln253Glu | missense_variant | 1.0 |
| rpsA | 1834303 | c.762T>G | synonymous_variant | 1.0 |
| rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
| rpsA | 1834307 | p.Asp256Asn | missense_variant | 1.0 |
| rpsA | 1834327 | c.786G>T | synonymous_variant | 1.0 |
| rpsA | 1834339 | c.798C>T | synonymous_variant | 1.0 |
| rpsA | 1834340 | p.Met267Leu | missense_variant | 1.0 |
| rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
| rpsA | 1834354 | c.813G>C | synonymous_variant | 1.0 |
| rpsA | 1834357 | c.816T>C | synonymous_variant | 1.0 |
| rpsA | 1834361 | c.820T>C | synonymous_variant | 1.0 |
| rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
| rpsA | 1834369 | c.828C>G | synonymous_variant | 1.0 |
| rpsA | 1834375 | c.834G>C | synonymous_variant | 1.0 |
| rpsA | 1834378 | c.837T>C | synonymous_variant | 1.0 |
| rpsA | 1834387 | c.846C>T | synonymous_variant | 1.0 |
| rpsA | 1834399 | p.His286Gln | missense_variant | 1.0 |
| rpsA | 1834405 | c.864C>T | synonymous_variant | 1.0 |
| rpsA | 1834408 | c.867C>T | synonymous_variant | 1.0 |
| rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
| rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
| rpsA | 1834435 | c.894G>C | synonymous_variant | 1.0 |
| rpsA | 1834438 | c.897C>T | synonymous_variant | 1.0 |
| rpsA | 1834451 | c.910T>C | synonymous_variant | 1.0 |
| rpsA | 1834459 | c.918G>C | synonymous_variant | 1.0 |
| rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
| rpsA | 1834480 | c.939C>G | synonymous_variant | 1.0 |
| rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
| rpsA | 1834498 | c.957C>T | synonymous_variant | 1.0 |
| rpsA | 1834519 | c.978G>C | synonymous_variant | 1.0 |
| rpsA | 1834528 | c.987T>G | synonymous_variant | 1.0 |
| rpsA | 1834531 | c.990C>T | synonymous_variant | 1.0 |
| rpsA | 1834540 | c.999G>C | synonymous_variant | 1.0 |
| rpsA | 1834543 | c.1002C>G | synonymous_variant | 1.0 |
| rpsA | 1834552 | c.1011G>C | synonymous_variant | 1.0 |
| rpsA | 1834555 | c.1014T>G | synonymous_variant | 1.0 |
| rpsA | 1834557 | p.Ala339Val | missense_variant | 1.0 |
| rpsA | 1834591 | c.1050C>T | synonymous_variant | 1.0 |
| rpsA | 1834603 | c.1062G>A | synonymous_variant | 1.0 |
| rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
| rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
| rpsA | 1834663 | c.1122C>T | synonymous_variant | 1.0 |
| rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
| rpsA | 1834678 | c.1137C>T | synonymous_variant | 1.0 |
| rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
| rpsA | 1834733 | p.Ala398Pro | missense_variant | 1.0 |
| rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
| rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
| rpsA | 1834759 | c.1218A>C | synonymous_variant | 1.0 |
| rpsA | 1834765 | p.Glu408Asp | missense_variant | 1.0 |
| rpsA | 1834776 | p.Ala412Glu | missense_variant | 1.0 |
| rpsA | 1834780 | c.1239A>G | synonymous_variant | 1.0 |
| rpsA | 1834788 | p.Ala416Gly | missense_variant | 1.0 |
| rpsA | 1834792 | c.1251G>C | synonymous_variant | 1.0 |
| rpsA | 1834804 | c.1263C>G | synonymous_variant | 1.0 |
| katG | 2155691 | c.421T>C | synonymous_variant | 1.0 |
| katG | 2155695 | c.417C>G | synonymous_variant | 1.0 |
| katG | 2155716 | c.394_396delCTTinsTTG | synonymous_variant | 1.0 |
| katG | 2155728 | c.384G>T | synonymous_variant | 1.0 |
| katG | 2155737 | c.375C>T | synonymous_variant | 1.0 |
| katG | 2155743 | c.369G>C | synonymous_variant | 1.0 |
| katG | 2155746 | c.366C>G | synonymous_variant | 1.0 |
| katG | 2155752 | c.360C>T | synonymous_variant | 1.0 |
| katG | 2155755 | c.357C>G | synonymous_variant | 1.0 |
| kasA | 2517922 | c.-193_-192delCCinsTG | upstream_gene_variant | 1.0 |
| kasA | 2517950 | c.-165C>G | upstream_gene_variant | 1.0 |
| kasA | 2517959 | c.-156C>T | upstream_gene_variant | 1.0 |
| ahpC | 2726582 | c.390G>C | synonymous_variant | 1.0 |
| ahpC | 2726593 | p.Val134Ala | missense_variant | 1.0 |
| ahpC | 2726600 | c.408T>C | synonymous_variant | 1.0 |
| ahpC | 2726612 | c.420C>G | synonymous_variant | 1.0 |
| ahpC | 2726638 | p.Ala149Val | missense_variant | 1.0 |
| ahpC | 2726654 | c.462G>C | synonymous_variant | 1.0 |
| ahpC | 2726657 | c.465A>C | synonymous_variant | 1.0 |
| ahpC | 2726663 | c.471C>T | synonymous_variant | 1.0 |
| ahpC | 2726669 | c.477T>C | synonymous_variant | 1.0 |
| ahpC | 2726675 | c.483A>G | synonymous_variant | 1.0 |
| ahpC | 2726681 | c.489A>C | synonymous_variant | 1.0 |
| ahpC | 2726684 | c.492G>A | synonymous_variant | 1.0 |
| ahpC | 2726687 | c.495C>G | synonymous_variant | 1.0 |
| ahpC | 2726693 | c.501C>G | synonymous_variant | 1.0 |
| ahpC | 2726696 | c.504C>G | synonymous_variant | 1.0 |
| ahpC | 2726708 | c.516G>A | synonymous_variant | 1.0 |
| ribD | 2986915 | p.Gly26Asp | missense_variant | 1.0 |
| rpoA | 3877557 | c.951C>G | synonymous_variant | 1.0 |
| rpoA | 3877567 | c.940_941delAGinsTC | synonymous_variant | 1.0 |
| rpoA | 3877571 | p.Pro313Ala | missense_variant | 1.0 |
| rpoA | 3877587 | c.921A>G | synonymous_variant | 1.0 |
| rpoA | 3877590 | c.918G>C | synonymous_variant | 1.0 |
| rpoA | 3877600 | p.Gln303Ala | missense_variant | 1.0 |
| rpoA | 3877613 | p.Ile299Val | missense_variant | 1.0 |
| rpoA | 3877617 | c.891G>C | synonymous_variant | 1.0 |
| rpoA | 3877638 | c.870T>C | synonymous_variant | 1.0 |
| rpoA | 3877647 | c.861C>T | synonymous_variant | 1.0 |
| rpoA | 3877653 | c.855C>T | synonymous_variant | 1.0 |
| rpoA | 3877656 | c.852T>G | synonymous_variant | 1.0 |
| rpoA | 3877662 | c.846C>T | synonymous_variant | 1.0 |
| rpoA | 3877665 | c.843C>G | synonymous_variant | 0.89 |
| rpoA | 3877677 | c.831G>A | synonymous_variant | 1.0 |
| rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
| rpoA | 3877692 | c.816G>C | synonymous_variant | 1.0 |
| rpoA | 3877704 | c.804G>T | synonymous_variant | 1.0 |
| rpoA | 3877716 | c.792C>G | synonymous_variant | 1.0 |
| rpoA | 3877734 | c.774G>C | synonymous_variant | 1.0 |
| rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
| rpoA | 3877749 | c.759C>T | synonymous_variant | 1.0 |
| rpoA | 3877752 | p.Asp252Glu | missense_variant | 1.0 |
| rpoA | 3877764 | p.Ala248Gly | missense_variant | 1.0 |
| rpoA | 3877770 | c.738A>C | synonymous_variant | 1.0 |
| rpoA | 3877773 | c.735G>C | synonymous_variant | 1.0 |
| rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
| rpoA | 3877785 | c.723C>G | synonymous_variant | 1.0 |
| rpoA | 3877797 | c.711G>C | synonymous_variant | 1.0 |
| rpoA | 3877803 | c.705G>C | synonymous_variant | 1.0 |
| rpoA | 3877824 | c.684G>A | synonymous_variant | 1.0 |
| rpoA | 3877833 | c.675C>G | synonymous_variant | 1.0 |
| rpoA | 3877836 | c.672A>G | synonymous_variant | 1.0 |
| rpoA | 3877839 | c.669G>T | synonymous_variant | 1.0 |
| rpoA | 3877842 | c.666A>C | synonymous_variant | 1.0 |
| rpoA | 3877856 | c.652T>C | synonymous_variant | 1.0 |
| rpoA | 3877857 | c.651G>A | synonymous_variant | 1.0 |
| rpoA | 3877866 | c.642G>C | synonymous_variant | 1.0 |
| rpoA | 3877875 | c.633T>G | synonymous_variant | 1.0 |
| rpoA | 3877881 | c.627G>C | synonymous_variant | 1.0 |
| rpoA | 3877884 | c.624G>C | synonymous_variant | 1.0 |
| rpoA | 3877893 | c.615C>G | synonymous_variant | 1.0 |
| rpoA | 3877898 | p.Pro204Ala | missense_variant | 1.0 |
| rpoA | 3877905 | c.603A>C | synonymous_variant | 1.0 |
| rpoA | 3877908 | c.600T>C | synonymous_variant | 1.0 |
| rpoA | 3877932 | c.576G>C | synonymous_variant | 1.0 |
| rpoA | 3877936 | p.Lys191Arg | missense_variant | 1.0 |
| rpoA | 3877956 | c.552G>A | synonymous_variant | 1.0 |
| rpoA | 3877962 | c.546G>T | synonymous_variant | 1.0 |
| rpoA | 3877971 | p.Asp179Glu | missense_variant | 1.0 |
| rpoA | 3877974 | c.534G>C | synonymous_variant | 1.0 |
| rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
| rpoA | 3878001 | c.507A>G | synonymous_variant | 1.0 |
| rpoA | 3878010 | c.498C>G | synonymous_variant | 1.0 |
| rpoA | 3878205 | c.303T>C | synonymous_variant | 1.0 |
| rpoA | 3878217 | c.291A>G | synonymous_variant | 1.0 |
| rpoA | 3878244 | c.264G>A | synonymous_variant | 1.0 |
| rpoA | 3878247 | c.261G>C | synonymous_variant | 1.0 |
| rpoA | 3878256 | c.252G>C | synonymous_variant | 1.0 |
| rpoA | 3878264 | p.Ser82Gly | missense_variant | 1.0 |
| rpoA | 3878271 | c.237T>C | synonymous_variant | 1.0 |
| rpoA | 3878283 | p.Glu75Asp | missense_variant | 1.0 |
| clpC1 | 4038755 | c.1950G>C | synonymous_variant | 1.0 |
| clpC1 | 4038767 | c.1938G>C | synonymous_variant | 1.0 |
| clpC1 | 4038773 | c.1932T>C | synonymous_variant | 1.0 |
| clpC1 | 4038790 | c.1915C>T | synonymous_variant | 1.0 |
| clpC1 | 4038795 | p.Ser637Thr | missense_variant | 1.0 |
| clpC1 | 4038812 | c.1893T>C | synonymous_variant | 1.0 |
| clpC1 | 4038815 | c.1890G>C | synonymous_variant | 1.0 |
| clpC1 | 4038821 | c.1884G>A | synonymous_variant | 1.0 |
| clpC1 | 4038860 | c.1845G>C | synonymous_variant | 1.0 |
| clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
| clpC1 | 4038884 | c.1821C>T | synonymous_variant | 1.0 |
| clpC1 | 4038887 | c.1818G>A | synonymous_variant | 1.0 |
| clpC1 | 4038905 | c.1800A>C | synonymous_variant | 1.0 |
| clpC1 | 4038908 | c.1797C>G | synonymous_variant | 1.0 |
| clpC1 | 4038911 | c.1794G>T | synonymous_variant | 1.0 |
| clpC1 | 4038914 | c.1791G>C | synonymous_variant | 1.0 |
| clpC1 | 4038917 | c.1788C>T | synonymous_variant | 1.0 |
| clpC1 | 4038923 | c.1782A>G | synonymous_variant | 1.0 |
| clpC1 | 4038932 | c.1773G>C | synonymous_variant | 1.0 |
| clpC1 | 4038941 | c.1764G>C | synonymous_variant | 1.0 |
| clpC1 | 4038953 | c.1752A>G | synonymous_variant | 1.0 |
| clpC1 | 4038956 | c.1749T>C | synonymous_variant | 1.0 |
| clpC1 | 4038962 | c.1743C>T | synonymous_variant | 1.0 |
| clpC1 | 4038965 | c.1740T>C | synonymous_variant | 1.0 |
| clpC1 | 4038971 | c.1734T>C | synonymous_variant | 1.0 |
| clpC1 | 4038974 | c.1731T>C | synonymous_variant | 1.0 |
| clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
| clpC1 | 4038995 | c.1708_1710delTTGinsCTC | synonymous_variant | 1.0 |
| clpC1 | 4039004 | c.1701C>G | synonymous_variant | 1.0 |
| clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
| clpC1 | 4039046 | c.1659C>T | synonymous_variant | 1.0 |
| clpC1 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
| clpC1 | 4039067 | c.1638G>C | synonymous_variant | 1.0 |
| clpC1 | 4039079 | c.1626C>G | synonymous_variant | 1.0 |
| clpC1 | 4039082 | c.1623C>T | synonymous_variant | 1.0 |
| clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
| clpC1 | 4039091 | c.1614G>T | synonymous_variant | 1.0 |
| clpC1 | 4039097 | c.1608G>C | synonymous_variant | 1.0 |
| clpC1 | 4039106 | c.1599G>C | synonymous_variant | 1.0 |
| clpC1 | 4039118 | c.1587C>G | synonymous_variant | 1.0 |
| clpC1 | 4039121 | c.1584T>G | synonymous_variant | 1.0 |
| clpC1 | 4039133 | c.1572C>G | synonymous_variant | 1.0 |
| clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.83 |
| clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.86 |
| clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.83 |
| clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.86 |
| clpC1 | 4039178 | c.1527G>T | synonymous_variant | 0.86 |
| clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 0.86 |
| clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.83 |
| clpC1 | 4039220 | c.1485G>C | synonymous_variant | 0.67 |
| clpC1 | 4039239 | p.Gly489Ala | missense_variant | 0.75 |
| clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
| clpC1 | 4039448 | c.1257A>G | synonymous_variant | 1.0 |
| clpC1 | 4039454 | c.1251A>C | synonymous_variant | 1.0 |
| clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
| clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
| clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
| clpC1 | 4039472 | c.1233G>T | synonymous_variant | 1.0 |
| clpC1 | 4039481 | c.1224T>C | synonymous_variant | 1.0 |
| clpC1 | 4039484 | c.1221T>C | synonymous_variant | 1.0 |
| clpC1 | 4039487 | c.1218G>C | synonymous_variant | 1.0 |
| clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
| clpC1 | 4039544 | c.1161C>T | synonymous_variant | 1.0 |
| clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
| clpC1 | 4039571 | c.1134G>A | synonymous_variant | 1.0 |
| clpC1 | 4039574 | p.Ala377Gly | missense_variant | 1.0 |
| clpC1 | 4039586 | c.1119G>C | synonymous_variant | 1.0 |
| clpC1 | 4039589 | c.1116G>C | synonymous_variant | 1.0 |
| clpC1 | 4039595 | c.1110C>T | synonymous_variant | 1.0 |
| clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
| clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
| clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
| clpC1 | 4039634 | p.Glu357Asn | missense_variant | 1.0 |
| clpC1 | 4039649 | c.1056G>C | synonymous_variant | 1.0 |
| clpC1 | 4039652 | c.1053G>C | synonymous_variant | 1.0 |
| clpC1 | 4039661 | c.1044T>C | synonymous_variant | 1.0 |
| clpC1 | 4039691 | c.1014G>C | synonymous_variant | 1.0 |
| clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
| clpC1 | 4039697 | c.1008C>G | synonymous_variant | 1.0 |
| clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
| clpC1 | 4039739 | c.966C>G | synonymous_variant | 1.0 |
| clpC1 | 4039742 | c.963C>T | synonymous_variant | 1.0 |
| clpC1 | 4039748 | c.957G>C | synonymous_variant | 1.0 |
| clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
| clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
| clpC1 | 4039760 | c.945T>C | synonymous_variant | 1.0 |
| clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
| clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
| clpC1 | 4039793 | c.912C>G | synonymous_variant | 1.0 |
| clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
| clpC1 | 4039820 | c.885T>C | synonymous_variant | 1.0 |
| clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
| clpC1 | 4039840 | c.865C>T | synonymous_variant | 1.0 |
| clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
| clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
| clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
| clpC1 | 4039901 | c.804C>T | synonymous_variant | 1.0 |
| clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
| clpC1 | 4039907 | c.798G>A | synonymous_variant | 1.0 |
| clpC1 | 4039913 | c.792C>T | synonymous_variant | 1.0 |
| clpC1 | 4039925 | c.780C>T | synonymous_variant | 1.0 |
| clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
| clpC1 | 4039934 | c.771G>C | synonymous_variant | 1.0 |
| clpC1 | 4039937 | c.768G>C | synonymous_variant | 1.0 |
| clpC1 | 4039946 | c.759A>T | synonymous_variant | 1.0 |
| clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
| clpC1 | 4039955 | c.750G>C | synonymous_variant | 1.0 |
| clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
| clpC1 | 4039961 | c.744C>T | synonymous_variant | 1.0 |
| clpC1 | 4039988 | c.717C>G | synonymous_variant | 1.0 |
| clpC1 | 4039997 | c.708C>T | synonymous_variant | 1.0 |
| clpC1 | 4040002 | p.His235Asn | missense_variant | 1.0 |
| clpC1 | 4040003 | c.702G>C | synonymous_variant | 1.0 |
| clpC1 | 4040009 | c.696C>G | synonymous_variant | 1.0 |
| clpC1 | 4040015 | c.690G>C | synonymous_variant | 1.0 |
| clpC1 | 4040018 | c.687G>C | synonymous_variant | 1.0 |
| clpC1 | 4040021 | c.684A>G | synonymous_variant | 1.0 |
| clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
| clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
| clpC1 | 4040042 | c.663C>T | synonymous_variant | 1.0 |
| clpC1 | 4040045 | c.660C>G | synonymous_variant | 1.0 |
| clpC1 | 4040057 | c.648C>T | synonymous_variant | 1.0 |
| clpC1 | 4040072 | c.633C>T | synonymous_variant | 1.0 |
| clpC1 | 4040087 | c.618G>C | synonymous_variant | 1.0 |
| clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 1.0 |
| clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
| clpC1 | 4040124 | p.Glu194Ser | missense_variant | 1.0 |
| clpC1 | 4040129 | c.576C>T | synonymous_variant | 1.0 |
| clpC1 | 4040144 | c.561G>C | synonymous_variant | 1.0 |
| clpC1 | 4040153 | c.552A>G | synonymous_variant | 1.0 |
| clpC1 | 4040158 | p.Met183Leu | missense_variant | 1.0 |
| clpC1 | 4040159 | c.546G>C | synonymous_variant | 1.0 |
| clpC1 | 4040162 | c.543G>C | synonymous_variant | 1.0 |
| clpC1 | 4040166 | p.Ala180Gln | missense_variant | 1.0 |
| clpC1 | 4040168 | c.537G>C | synonymous_variant | 1.0 |
| clpC1 | 4040444 | c.261C>G | synonymous_variant | 1.0 |
| clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
| clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
| clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
| clpC1 | 4040474 | c.231C>T | synonymous_variant | 1.0 |
| clpC1 | 4040477 | c.228G>C | synonymous_variant | 1.0 |
| clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
| clpC1 | 4040486 | c.219G>C | synonymous_variant | 1.0 |
| clpC1 | 4040495 | c.210C>G | synonymous_variant | 1.0 |
| clpC1 | 4040501 | c.204C>T | synonymous_variant | 1.0 |
| clpC1 | 4040531 | c.174T>C | synonymous_variant | 1.0 |
| clpC1 | 4040534 | c.171A>G | synonymous_variant | 1.0 |
| clpC1 | 4040539 | c.166C>T | synonymous_variant | 1.0 |
