Run ID: ERR4815944
Sample name:
Date: 01-04-2023 14:09:07
Number of reads: 391753
Percentage reads mapped: 84.9
Strain: lineage4.1.2.1
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 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155650 | c.461delA | frameshift_variant | 0.29 | isoniazid |
embB | 4247586 | p.Gly358Val | missense_variant | 0.14 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5415 | p.Ala59Val | missense_variant | 0.33 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7901 | c.600G>A | synonymous_variant | 0.33 |
gyrA | 9283 | p.Gly661Asp | missense_variant | 0.22 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490694 | c.-89G>C | upstream_gene_variant | 0.4 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 620814 | c.924C>T | synonymous_variant | 0.12 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760197 | p.Ala131Thr | missense_variant | 0.22 |
rpoB | 760872 | p.Glu356* | stop_gained | 0.33 |
rpoB | 761767 | p.Val654Gly | missense_variant | 0.25 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.2 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.25 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.36 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.33 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.33 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.31 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.31 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.27 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.25 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.25 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.22 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.22 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.22 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.22 |
rpoC | 763570 | c.201G>T | synonymous_variant | 0.29 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.22 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.22 |
rpoC | 763609 | c.240C>T | synonymous_variant | 0.29 |
rpoC | 763619 | p.Arg84Lys | missense_variant | 0.2 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.22 |
rpoC | 763642 | c.273G>T | synonymous_variant | 0.25 |
rpoC | 763654 | c.285C>T | synonymous_variant | 0.29 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.33 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.33 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.33 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.25 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.25 |
rpoC | 764424 | p.Asn352Thr | missense_variant | 0.15 |
rpoC | 764428 | c.1059G>A | synonymous_variant | 0.17 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.15 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.23 |
rpoC | 764435 | c.1066_1068delAGGinsCGT | synonymous_variant | 0.31 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.23 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 0.13 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.24 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.24 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.13 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.15 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.15 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.2 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766167 | p.Ala933Val | missense_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776143 | p.Gly780Arg | missense_variant | 0.17 |
mmpL5 | 776516 | c.1964delT | frameshift_variant | 0.15 |
mmpL5 | 777648 | p.Ala278Val | missense_variant | 0.15 |
mmpS5 | 778768 | c.136_137delGA | frameshift_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781485 | c.-75C>A | upstream_gene_variant | 0.12 |
Rv1258c | 1406089 | p.Ala418Thr | missense_variant | 0.18 |
atpE | 1461196 | p.Thr51Lys | missense_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472954 | n.1109T>C | 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 | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473122 | n.1281delA | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473122 | n.1278A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473291 | n.1446G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475767 | n.2110_2111insT | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1673322 | c.-118C>G | upstream_gene_variant | 0.4 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.5 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.5 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.4 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155403 | p.Gly237Ser | missense_variant | 0.22 |
katG | 2156396 | c.-285C>T | upstream_gene_variant | 0.22 |
PPE35 | 2170226 | c.386delA | frameshift_variant | 1.0 |
Rv1979c | 2222394 | c.771G>T | synonymous_variant | 0.17 |
Rv1979c | 2222443 | p.Ala241Asp | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290114 | c.-873T>C | upstream_gene_variant | 0.33 |
pncA | 2290225 | c.-987_-985delGTT | upstream_gene_variant | 0.67 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518840 | c.726C>T | synonymous_variant | 0.18 |
pepQ | 2859401 | p.Asp340Asn | missense_variant | 0.12 |
thyX | 3067199 | c.747A>G | synonymous_variant | 0.15 |
thyA | 3073790 | p.Pro228Thr | missense_variant | 0.14 |
thyA | 3073821 | c.651G>A | synonymous_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448537 | p.Ala12Pro | missense_variant | 0.33 |
Rv3083 | 3449250 | c.747C>T | synonymous_variant | 0.17 |
Rv3083 | 3449700 | c.1197C>A | synonymous_variant | 0.15 |
Rv3083 | 3449739 | p.His412Gln | missense_variant | 0.14 |
Rv3083 | 3449792 | p.Ala430Val | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475131 | c.1125C>A | synonymous_variant | 0.29 |
fprA | 3475202 | p.Pro399Gln | missense_variant | 0.2 |
Rv3236c | 3612097 | c.1020C>T | synonymous_variant | 0.22 |
Rv3236c | 3613001 | p.Ala39Val | missense_variant | 0.25 |
fbiB | 3642746 | c.1212C>A | synonymous_variant | 0.18 |
rpoA | 3878132 | p.Ala126Ser | missense_variant | 0.2 |
clpC1 | 4039018 | p.Ser563Ala | missense_variant | 0.2 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.22 |
clpC1 | 4039042 | p.Ser555Thr | missense_variant | 0.15 |
clpC1 | 4040624 | c.80delA | frameshift_variant | 0.25 |
clpC1 | 4040753 | c.-49G>T | upstream_gene_variant | 0.2 |
embC | 4240045 | p.Trp61* | stop_gained | 0.22 |
embC | 4240875 | p.Ser338Asn | missense_variant | 0.22 |
embC | 4242307 | c.2446delA | frameshift_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embC | 4242941 | p.His1027Asp | missense_variant | 0.25 |
embA | 4244693 | c.1463delA | frameshift_variant | 0.22 |
embA | 4245272 | c.2040G>A | synonymous_variant | 0.11 |
embB | 4247071 | c.562delG | frameshift_variant | 0.18 |
embB | 4247263 | c.757_759delCTC | conservative_inframe_deletion | 0.2 |
embB | 4249015 | c.2502C>T | synonymous_variant | 0.17 |
ethA | 4326504 | p.Gly324Arg | missense_variant | 0.67 |
ethR | 4327702 | p.Lys52Gln | missense_variant | 0.5 |
ethA | 4328251 | c.-780_-779delCT | upstream_gene_variant | 0.14 |
whiB6 | 4338596 | c.-75G>C | upstream_gene_variant | 1.0 |