Run ID: SRR3732584
Sample name:
Date: 04-04-2023 05:36:09
Number of reads: 683392
Percentage reads mapped: 99.42
Strain: lineage4.3.3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
tlyA | 1918634 | p.Gly232Asp | missense_variant | 1.0 | capreomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
katG | 2155270 | p.Ala281Val | missense_variant | 0.25 | isoniazid |
pncA | 2289213 | p.Gln10Arg | missense_variant | 1.0 | pyrazinamide |
embB | 4247469 | p.Tyr319Ser | missense_variant | 1.0 | ethambutol |
gid | 4407952 | p.Pro84Leu | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6082 | p.Lys281Asn | missense_variant | 0.33 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7947 | p.Leu216Met | missense_variant | 0.4 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490674 | c.-109G>T | upstream_gene_variant | 0.14 |
fgd1 | 490698 | c.-85G>A | upstream_gene_variant | 0.17 |
fgd1 | 491289 | c.507C>A | synonymous_variant | 0.33 |
mshA | 575322 | c.-26C>A | upstream_gene_variant | 0.2 |
rpoB | 760152 | p.Cys116Ser | missense_variant | 0.67 |
rpoB | 760480 | p.Arg225Leu | missense_variant | 0.2 |
rpoB | 760556 | p.Glu250Asp | missense_variant | 0.22 |
rpoB | 762276 | p.Arg824Ser | missense_variant | 0.25 |
rpoB | 762639 | p.Gly945Trp | missense_variant | 0.29 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.5 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765072 | p.Pro568Leu | missense_variant | 0.18 |
rpoC | 765621 | c.2258_2259delCG | frameshift_variant | 0.67 |
rpoC | 766520 | p.Gly1051Ser | missense_variant | 0.22 |
rpoC | 766720 | c.3351C>T | synonymous_variant | 0.4 |
mmpL5 | 776565 | p.Pro639His | missense_variant | 0.5 |
mmpR5 | 778406 | c.-584G>T | upstream_gene_variant | 0.25 |
mmpS5 | 778748 | p.Pro53His | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801054 | c.246G>T | synonymous_variant | 0.67 |
rplC | 801188 | p.Met127Thr | missense_variant | 0.22 |
rplC | 801198 | c.390C>T | synonymous_variant | 0.2 |
fbiC | 1303161 | c.231G>A | synonymous_variant | 0.33 |
fbiC | 1305129 | c.2199C>A | synonymous_variant | 0.33 |
Rv1258c | 1406924 | c.416delT | frameshift_variant | 0.29 |
Rv1258c | 1407517 | c.-177G>T | upstream_gene_variant | 0.33 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473969 | n.312G>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834772 | p.Arg411Ser | missense_variant | 0.5 |
rpsA | 1834921 | c.1380G>A | synonymous_variant | 0.4 |
rpsA | 1834985 | c.1445dupG | frameshift_variant&stop_lost&splice_region_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102593 | c.450C>T | synonymous_variant | 0.33 |
katG | 2156354 | c.-243G>T | upstream_gene_variant | 1.0 |
katG | 2156449 | c.-338G>T | upstream_gene_variant | 0.5 |
PPE35 | 2167824 | p.Gly930Val | missense_variant | 0.5 |
PPE35 | 2168506 | p.Gly703Ser | missense_variant | 0.5 |
Rv1979c | 2222820 | c.345G>T | synonymous_variant | 0.4 |
Rv1979c | 2222970 | c.195C>T | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289671 | c.-430G>T | upstream_gene_variant | 0.25 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
eis | 2714871 | c.462G>T | synonymous_variant | 0.33 |
eis | 2715218 | p.Leu39Met | missense_variant | 0.2 |
eis | 2715471 | c.-139C>A | upstream_gene_variant | 0.33 |
eis | 2715550 | c.-218G>T | upstream_gene_variant | 0.25 |
eis | 2715578 | c.-247delG | upstream_gene_variant | 0.25 |
folC | 2747262 | p.Lys113* | stop_gained | 0.33 |
ribD | 2986772 | c.-67C>T | upstream_gene_variant | 0.29 |
Rv2752c | 3065376 | c.816C>A | synonymous_variant | 0.5 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3073977 | c.490_494delTACCA | frameshift_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339058 | c.-60G>T | upstream_gene_variant | 0.2 |
Rv3083 | 3448319 | c.-185_-184insG | upstream_gene_variant | 0.33 |
Rv3083 | 3448850 | p.Trp116Leu | missense_variant | 0.4 |
Rv3083 | 3449403 | c.900G>A | synonymous_variant | 0.4 |
Rv3083 | 3449745 | c.1242C>T | synonymous_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568532 | p.Arg50Trp | missense_variant | 0.4 |
Rv3236c | 3612298 | c.819C>A | synonymous_variant | 0.2 |
Rv3236c | 3612345 | p.Arg258Trp | missense_variant | 0.4 |
fbiA | 3640705 | p.Gly55Trp | missense_variant | 0.4 |
fbiA | 3641297 | p.Leu252Ser | missense_variant | 0.22 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040494 | p.Gln71Lys | missense_variant | 0.5 |
embC | 4240255 | c.393G>T | synonymous_variant | 0.4 |
embC | 4241658 | p.Ser599* | stop_gained | 0.33 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embA | 4244364 | p.Gly378Ser | missense_variant | 0.29 |
embA | 4244506 | p.Gly425Val | missense_variant | 0.29 |
embA | 4244568 | p.Arg446Cys | missense_variant | 0.22 |
embA | 4245312 | p.Ala694Thr | missense_variant | 0.67 |
embB | 4246499 | c.-15G>A | upstream_gene_variant | 0.29 |
embB | 4246642 | c.129G>T | synonymous_variant | 0.5 |
aftB | 4267312 | p.Gly509Trp | missense_variant | 0.29 |
aftB | 4268190 | p.Ala216Val | missense_variant | 0.5 |
aftB | 4268735 | c.102C>A | synonymous_variant | 0.67 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |