Run ID: ERR4816729
Sample name:
Date: 01-04-2023 14:35:43
Number of reads: 16715
Percentage reads mapped: 2.47
Strain: lineage4.9
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 760208 | p.Ile134Met | missense_variant | 1.0 |
rpoB | 760233 | c.427_429delAGTinsTCC | synonymous_variant | 1.0 |
rpoB | 760244 | c.438G>C | synonymous_variant | 1.0 |
rpoB | 760253 | c.447T>C | synonymous_variant | 1.0 |
rpoB | 760263 | p.Met153Leu | missense_variant | 1.0 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 1.0 |
rpoB | 760290 | p.Ile162Val | missense_variant | 1.0 |
rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
rpoB | 760301 | c.495C>A | synonymous_variant | 1.0 |
rpoB | 761207 | c.1401C>A | synonymous_variant | 1.0 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 1.0 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 1.0 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
rpoB | 761255 | c.1449T>C | synonymous_variant | 1.0 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 1.0 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 1.0 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 1.0 |
rpoB | 761276 | c.1470G>C | synonymous_variant | 1.0 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 1.0 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 1.0 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
rpoB | 762245 | c.2439G>T | synonymous_variant | 1.0 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 1.0 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
rpoB | 762273 | p.Ala823Ser | missense_variant | 1.0 |
rpoB | 762278 | c.2472C>T | synonymous_variant | 1.0 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 1.0 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 1.0 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 1.0 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 1.0 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 1.0 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 1.0 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 1.0 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 1.0 |
rpoC | 762929 | c.-441G>A | 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 | 762980 | c.-390T>C | upstream_gene_variant | 1.0 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 1.0 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 1.0 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 1.0 |
rpoC | 763085 | c.-285C>T | upstream_gene_variant | 1.0 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
rpoC | 763100 | c.-270G>A | 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 |
rpoB | 763122 | p.Ile1106Leu | missense_variant | 1.0 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
rpoB | 763130 | p.Glu1108Asp | missense_variant | 1.0 |
rpoC | 763136 | c.-234C>G | upstream_gene_variant | 1.0 |
rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
rpoC | 763483 | c.114G>C | synonymous_variant | 1.0 |
rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
rpoC | 763504 | c.135C>A | synonymous_variant | 1.0 |
rpoC | 763507 | c.138G>C | synonymous_variant | 1.0 |
rpoC | 763528 | c.159G>T | 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>T | synonymous_variant | 1.0 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
rpoC | 763621 | c.252C>T | synonymous_variant | 1.0 |
rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
rpoC | 763642 | c.273G>C | synonymous_variant | 1.0 |
rpoC | 763660 | c.291T>C | synonymous_variant | 1.0 |
rpoC | 763666 | c.297G>T | synonymous_variant | 1.0 |
rpoC | 763696 | c.327T>C | synonymous_variant | 1.0 |
rpoC | 763699 | c.330G>C | synonymous_variant | 1.0 |
rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
rpoC | 763709 | c.340C>T | synonymous_variant | 1.0 |
rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
rpoC | 763729 | c.360G>C | synonymous_variant | 1.0 |
rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
rpoC | 763751 | p.Ile128Val | missense_variant | 1.0 |
rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
rpoC | 764335 | c.966G>C | synonymous_variant | 1.0 |
rpoC | 764344 | c.975C>T | synonymous_variant | 1.0 |
rpoC | 764353 | c.984G>C | synonymous_variant | 1.0 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 1.0 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
rpoC | 764383 | c.1014C>T | synonymous_variant | 1.0 |
rpoC | 764386 | c.1017C>T | synonymous_variant | 1.0 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 1.0 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 1.0 |
rpoC | 764405 | c.1036_1038delAGGinsCGT | synonymous_variant | 1.0 |
rpoC | 764428 | c.1059G>T | 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.1066A>C | synonymous_variant | 1.0 |
rpoC | 764440 | c.1071G>C | synonymous_variant | 1.0 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 1.0 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 1.0 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 1.0 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 1.0 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 1.0 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 1.0 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 1.0 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
rpoC | 764524 | c.1155C>T | synonymous_variant | 1.0 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 1.0 |
rpoC | 764533 | c.1164C>A | synonymous_variant | 1.0 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 1.0 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 0.83 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 1.0 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 1.0 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
rpoC | 764582 | p.Leu405Met | missense_variant | 1.0 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 1.0 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 1.0 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
rpoC | 764679 | p.Lys437Ser | missense_variant | 1.0 |
rpoC | 764690 | p.Cys441Ala | missense_variant | 1.0 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
rpoC | 764808 | p.Arg480His | missense_variant | 1.0 |
rpoC | 764812 | c.1443C>G | 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 |
rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
rpsL | 781772 | c.213C>A | synonymous_variant | 1.0 |
rpsL | 781796 | p.Met79Ile | missense_variant | 1.0 |
rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
rpsL | 781805 | c.246G>C | synonymous_variant | 1.0 |
rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
rpsL | 781820 | c.261G>C | synonymous_variant | 1.0 |
rpsL | 781829 | c.270G>C | synonymous_variant | 1.0 |
rpsL | 781832 | c.273T>G | synonymous_variant | 1.0 |
rplC | 800618 | c.-191T>G | upstream_gene_variant | 1.0 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.75 |
rplC | 800645 | c.-164C>T | upstream_gene_variant | 0.75 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.75 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.75 |
rplC | 800667 | c.-142_-140delTCGinsAGC | upstream_gene_variant | 0.75 |
rplC | 800672 | c.-137G>T | upstream_gene_variant | 0.75 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.75 |
rplC | 800702 | c.-107G>T | upstream_gene_variant | 0.75 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.6 |
rrs | 1471967 | n.122G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471980 | n.135G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471981 | n.136C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471997 | n.152T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472023 | n.178G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472028 | n.183A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472030 | n.185G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472092 | n.247C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472102 | n.257G>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 | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472120 | n.275G>A | 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 | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473047 | n.1202C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473122 | n.1281delA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473157 | n.1312C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473164 | n.1319C>A | 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 | 1473843 | n.186G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473884 | n.227C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473887 | n.230T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473889 | n.232G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473898 | n.241C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474181 | n.524C>T | 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 | 1474202 | n.545T>C | 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 | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474356 | n.699T>C | 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 | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474806 | n.1149A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474822 | n.1165G>T | 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 | 1.0 |
rrl | 1474905 | n.1248T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475760 | n.2105_2106delGC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>T | 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 | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 1.0 |
rpsA | 1833676 | c.135A>G | 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 | 1833698 | p.Leu53Val | missense_variant | 1.0 |
rpsA | 1833709 | c.168C>A | synonymous_variant | 1.0 |
rpsA | 1833718 | c.177C>G | synonymous_variant | 1.0 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
rpsA | 1833959 | p.Leu140Val | missense_variant | 1.0 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 1.0 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 1.0 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
rpsA | 1834240 | c.699T>A | synonymous_variant | 1.0 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834255 | c.714C>G | synonymous_variant | 1.0 |
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 | 1834327 | c.786G>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.820_822delTTGinsCTC | synonymous_variant | 1.0 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 1.0 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 1.0 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 1.0 |
rpsA | 1834405 | c.864C>G | synonymous_variant | 1.0 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
rpsA | 1834416 | p.Ala292Val | missense_variant | 1.0 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 1.0 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 1.0 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 1.0 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 1.0 |
Rv3236c | 3612866 | p.Ser84Asn | missense_variant | 1.0 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 1.0 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 1.0 |
clpC1 | 4039736 | c.969C>G | synonymous_variant | 1.0 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 1.0 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 1.0 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 1.0 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 1.0 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 1.0 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 1.0 |
clpC1 | 4039808 | c.897G>A | synonymous_variant | 1.0 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 1.0 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 1.0 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
clpC1 | 4039853 | c.852G>C | synonymous_variant | 1.0 |
clpC1 | 4039865 | c.840T>A | synonymous_variant | 1.0 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 1.0 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
clpC1 | 4039913 | c.792C>T | synonymous_variant | 1.0 |
clpC1 | 4039976 | p.Lys243Thr | missense_variant | 1.0 |
clpC1 | 4039982 | p.Thr241Ile | missense_variant | 1.0 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 1.0 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 1.0 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 1.0 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 1.0 |
clpC1 | 4040021 | c.684A>T | synonymous_variant | 1.0 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.86 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.8 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.8 |
clpC1 | 4040066 | c.639G>T | synonymous_variant | 0.8 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.8 |
clpC1 | 4040411 | c.294T>G | synonymous_variant | 1.0 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
clpC1 | 4040429 | c.274_276delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4040435 | c.270G>C | synonymous_variant | 1.0 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
clpC1 | 4040453 | c.252C>G | synonymous_variant | 1.0 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
clpC1 | 4040480 | c.223_225delTCTinsAGC | synonymous_variant | 1.0 |