Run ID: ERR1750938
Sample name:
Date: 31-03-2023 15:01:09
Number of reads: 920424
Percentage reads mapped: 83.27
Strain: lineage4.4.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247959 | p.Met482Ile | missense_variant | 0.4 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5940 | p.Ser234Asn | missense_variant | 0.2 |
gyrB | 6066 | p.Val276Ala | missense_variant | 0.29 |
gyrB | 6068 | p.Asp277Tyr | missense_variant | 0.29 |
gyrA | 6712 | c.-590G>T | upstream_gene_variant | 0.2 |
gyrB | 6927 | p.Leu563Trp | missense_variant | 0.27 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7806 | p.Arg169Trp | missense_variant | 0.33 |
gyrA | 8149 | p.Phe283Ser | missense_variant | 0.33 |
gyrA | 8188 | c.889delG | frameshift_variant | 0.4 |
gyrA | 8205 | p.Ile302Phe | missense_variant | 0.4 |
gyrA | 8283 | p.Ile328Phe | missense_variant | 0.33 |
gyrA | 9138 | p.Gln613Glu | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490751 | c.-32T>G | upstream_gene_variant | 0.35 |
fgd1 | 490962 | c.180T>C | synonymous_variant | 0.33 |
fgd1 | 491067 | p.Cys95Trp | missense_variant | 0.29 |
fgd1 | 491111 | p.Ala110Val | missense_variant | 0.67 |
fgd1 | 491271 | c.489C>T | synonymous_variant | 0.25 |
mshA | 576246 | p.Gly300Val | missense_variant | 0.29 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.67 |
ccsA | 620072 | p.Pro61His | missense_variant | 0.14 |
ccsA | 620241 | c.351C>A | synonymous_variant | 0.4 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.43 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.4 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.33 |
rpoB | 759843 | p.Pro13Ser | missense_variant | 0.29 |
rpoB | 759887 | c.81C>T | synonymous_variant | 0.33 |
rpoB | 762793 | c.2987_2988insA | frameshift_variant | 0.29 |
rpoB | 763045 | p.Gln1080Leu | missense_variant | 0.4 |
rpoC | 763082 | c.-288C>G | upstream_gene_variant | 0.4 |
rpoB | 763093 | p.Val1096Ala | missense_variant | 0.4 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.4 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.5 |
rpoC | 763376 | p.Asp3Asn | missense_variant | 0.67 |
rpoC | 763736 | p.Lys123* | stop_gained | 0.67 |
rpoC | 763950 | p.Arg194Leu | missense_variant | 0.15 |
rpoC | 764003 | p.Ala212Ser | missense_variant | 0.2 |
rpoC | 764038 | p.Trp223* | stop_gained | 0.18 |
rpoC | 764048 | c.681delC | frameshift_variant | 0.2 |
rpoC | 764062 | c.693C>A | synonymous_variant | 0.22 |
rpoC | 764549 | p.Pro394Thr | missense_variant | 0.17 |
rpoC | 766079 | p.Arg904Ser | missense_variant | 0.17 |
mmpL5 | 776738 | c.1743C>T | synonymous_variant | 0.67 |
mmpL5 | 776741 | c.1740C>T | synonymous_variant | 0.67 |
mmpL5 | 776744 | c.1737C>G | synonymous_variant | 0.67 |
mmpL5 | 776756 | p.Asp575Glu | missense_variant | 0.67 |
mmpL5 | 777250 | p.Tyr411Asn | missense_variant | 0.25 |
mmpL5 | 777254 | c.1227G>A | synonymous_variant | 0.22 |
mmpL5 | 777258 | p.Leu408Gln | missense_variant | 0.22 |
mmpL5 | 777416 | c.1065G>T | synonymous_variant | 0.94 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801287 | p.Val160Gly | missense_variant | 0.75 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.4 |
fbiC | 1303127 | p.Arg66Leu | missense_variant | 0.25 |
fbiC | 1304627 | p.Ala566Glu | missense_variant | 0.29 |
fbiC | 1305441 | c.2511C>T | synonymous_variant | 0.2 |
embR | 1417542 | c.-195C>A | upstream_gene_variant | 0.5 |
atpE | 1461086 | c.42A>G | synonymous_variant | 0.31 |
atpE | 1461101 | c.57T>G | synonymous_variant | 0.3 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472446 | n.601_602insTCTGCAA | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472449 | n.606_612delCGGCTTA | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472459 | n.614C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472463 | n.618G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472497 | n.652G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473097 | n.1252G>A | non_coding_transcript_exon_variant | 0.75 |
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 | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473134 | n.1289T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473147 | n.1302G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474021 | n.364A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474720 | n.1063C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474740 | n.1083G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474747 | n.1090C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475075 | n.1418A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475748 | n.2091G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475756 | n.2101_2108delACCCGCAA | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476156 | n.2499C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476178 | n.2521C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.83 |
fabG1 | 1673369 | c.-71A>T | upstream_gene_variant | 0.4 |
fabG1 | 1673932 | p.Arg165Cys | missense_variant | 0.4 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.4 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.4 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.4 |
rpsA | 1834483 | p.Glu314Asp | missense_variant | 0.4 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.4 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.33 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.33 |
rpsA | 1834531 | c.990C>T | synonymous_variant | 0.4 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 0.29 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.29 |
rpsA | 1834564 | c.1023C>T | synonymous_variant | 0.29 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.4 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.33 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.33 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.33 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.33 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.33 |
rpsA | 1834646 | p.Tyr369Asn | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918360 | p.Pro141Ser | missense_variant | 0.25 |
ndh | 2101754 | p.Thr430Ile | missense_variant | 0.29 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
ndh | 2103227 | c.-185T>C | upstream_gene_variant | 0.25 |
katG | 2154270 | c.1842G>A | synonymous_variant | 1.0 |
PPE35 | 2168429 | c.2184G>A | synonymous_variant | 0.18 |
PPE35 | 2168479 | p.Thr712Pro | missense_variant | 1.0 |
PPE35 | 2169559 | c.1052_1053delTG | frameshift_variant | 0.2 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2170304 | c.309G>A | synonymous_variant | 0.15 |
PPE35 | 2170585 | p.Ile10Phe | missense_variant | 0.2 |
PPE35 | 2170628 | c.-16C>T | upstream_gene_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288971 | p.Glu91Lys | missense_variant | 0.67 |
pncA | 2289019 | p.Gly75Ser | missense_variant | 0.67 |
kasA | 2518147 | c.33C>T | synonymous_variant | 0.4 |
kasA | 2518678 | c.564C>T | synonymous_variant | 0.4 |
kasA | 2518713 | p.Gly200Val | missense_variant | 0.5 |
eis | 2714844 | c.489C>A | synonymous_variant | 0.2 |
eis | 2714936 | p.Pro133Ser | missense_variant | 0.2 |
eis | 2714955 | c.378C>T | synonymous_variant | 0.2 |
eis | 2715103 | p.Leu77Pro | missense_variant | 0.3 |
eis | 2715229 | p.Ala35Val | missense_variant | 0.67 |
ahpC | 2726265 | p.Lys25Gln | missense_variant | 0.22 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.33 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.5 |
ahpC | 2726741 | c.549G>A | synonymous_variant | 0.25 |
folC | 2746380 | p.Gly407Trp | missense_variant | 0.4 |
pepQ | 2859524 | p.Gly299Cys | missense_variant | 0.33 |
pepQ | 2859606 | c.813G>T | synonymous_variant | 0.25 |
pepQ | 2859667 | c.750_751delTC | frameshift_variant | 0.25 |
pepQ | 2859736 | p.Gly228Glu | missense_variant | 0.25 |
Rv2752c | 3065724 | c.468C>T | synonymous_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339491 | p.Leu125His | missense_variant | 0.18 |
Rv3083 | 3448838 | p.Arg112Gln | missense_variant | 0.18 |
Rv3083 | 3448924 | p.Gly141Ser | missense_variant | 0.25 |
Rv3083 | 3449382 | p.Trp293Cys | missense_variant | 0.67 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475340 | p.Ala445Asp | missense_variant | 0.43 |
whiB7 | 3568779 | c.-100T>C | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
Rv3236c | 3612811 | c.306G>T | synonymous_variant | 0.4 |
Rv3236c | 3613083 | p.Gly12Cys | missense_variant | 0.22 |
fbiA | 3641203 | p.Gly221Cys | missense_variant | 0.67 |
fbiB | 3641418 | c.-117C>T | upstream_gene_variant | 0.4 |
fbiB | 3642169 | p.Thr212Lys | missense_variant | 0.29 |
fbiB | 3642595 | p.Pro354Leu | missense_variant | 0.33 |
fbiB | 3642705 | p.Arg391Ser | missense_variant | 0.18 |
fbiB | 3642732 | p.Ser400Thr | missense_variant | 0.15 |
rpoA | 3878175 | c.333G>T | synonymous_variant | 0.15 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 0.25 |
clpC1 | 4038223 | p.Ala828Ser | missense_variant | 0.33 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.5 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.6 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.67 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.8 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.8 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.75 |
clpC1 | 4038926 | c.1779G>T | synonymous_variant | 0.75 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.75 |
clpC1 | 4038944 | c.1761C>T | synonymous_variant | 0.75 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.75 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.75 |
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 | 4038980 | c.1725C>T | synonymous_variant | 1.0 |
clpC1 | 4038986 | p.Asp573Glu | missense_variant | 1.0 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 1.0 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 1.0 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 1.0 |
clpC1 | 4039019 | c.1686G>C | synonymous_variant | 1.0 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 1.0 |
clpC1 | 4039630 | p.Leu359Phe | missense_variant | 0.2 |
clpC1 | 4039999 | p.Gly236Ser | missense_variant | 0.25 |
panD | 4043987 | p.Arg99Cys | missense_variant | 0.5 |
embC | 4239973 | c.111T>G | synonymous_variant | 0.5 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.6 |
embC | 4240978 | p.Lys372Asn | missense_variant | 0.33 |
embA | 4242250 | c.-983C>A | upstream_gene_variant | 0.22 |
embA | 4243859 | c.627C>T | synonymous_variant | 0.22 |
embA | 4243861 | p.Gly210Asp | missense_variant | 0.22 |
embA | 4244058 | p.Tyr276Asn | missense_variant | 0.5 |
embA | 4244183 | c.951G>A | synonymous_variant | 0.25 |
embA | 4244222 | c.990G>T | synonymous_variant | 0.18 |
embA | 4244443 | p.Arg404Leu | missense_variant | 0.22 |
embA | 4244450 | c.1218C>T | synonymous_variant | 0.2 |
embB | 4247133 | p.Asp207Gly | missense_variant | 0.22 |
embB | 4247737 | c.1224C>T | synonymous_variant | 0.25 |
embB | 4247816 | p.Val435Ile | missense_variant | 0.2 |
embB | 4247921 | p.His470Tyr | missense_variant | 0.33 |
embB | 4248066 | p.Trp518* | stop_gained | 0.4 |
embB | 4249266 | p.Pro918Leu | missense_variant | 0.29 |
aftB | 4267230 | p.Trp536* | stop_gained | 0.5 |
ubiA | 4268965 | p.Ala290Glu | missense_variant | 0.67 |
ubiA | 4269406 | p.Lys143Leu | missense_variant | 0.5 |
ubiA | 4269646 | p.Ser63Ile | missense_variant | 0.14 |
ubiA | 4269859 | c.-26A>C | upstream_gene_variant | 0.25 |
ethA | 4328216 | c.-743C>T | upstream_gene_variant | 0.25 |
ethA | 4328257 | c.-784A>T | upstream_gene_variant | 0.29 |
ethA | 4328267 | c.-794G>T | upstream_gene_variant | 0.4 |
ethA | 4328328 | c.-855C>A | upstream_gene_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |