Run ID: SRR6045308
Sample name:
Date: 04-04-2023 11:56:38
Number of reads: 919125
Percentage reads mapped: 93.53
Strain: lineage3.1.2.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.2 | East-African-Indian | CAS;CAS2 | RD750 | 0.99 |
lineage3.1.2.2 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9611 | c.2310C>T | synonymous_variant | 1.0 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.27 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.33 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760446 | p.Asp214Tyr | missense_variant | 0.12 |
rpoB | 761933 | c.2127G>T | synonymous_variant | 0.12 |
rpoB | 762068 | c.2262C>T | synonymous_variant | 0.14 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777374 | p.Glu369Asp | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304573 | p.Val548Ala | missense_variant | 0.11 |
Rv1258c | 1407489 | c.-149G>A | upstream_gene_variant | 0.13 |
Rv1258c | 1407538 | c.-198T>C | upstream_gene_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474275 | n.618T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.3 |
fabG1 | 1674127 | p.Ser230Gly | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102204 | p.Val280Ala | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.14 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.13 |
PPE35 | 2168604 | p.Pro670Leu | missense_variant | 1.0 |
PPE35 | 2169002 | c.1611G>A | synonymous_variant | 0.13 |
PPE35 | 2170202 | c.411A>G | synonymous_variant | 0.15 |
PPE35 | 2170205 | c.408C>G | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518106 | c.-9C>G | upstream_gene_variant | 0.15 |
kasA | 2518147 | c.33C>T | synonymous_variant | 0.29 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.17 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.17 |
eis | 2714795 | p.Glu180Lys | missense_variant | 0.11 |
eis | 2715057 | c.276C>T | synonymous_variant | 0.17 |
eis | 2715060 | p.His91Met | missense_variant | 0.17 |
eis | 2715065 | p.Thr90Ala | missense_variant | 0.15 |
eis | 2715469 | c.-137T>C | upstream_gene_variant | 0.13 |
eis | 2715473 | c.-141A>G | upstream_gene_variant | 0.13 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.29 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.21 |
folC | 2746453 | c.1146G>A | synonymous_variant | 0.14 |
ribD | 2987250 | p.Met138Leu | missense_variant | 0.15 |
Rv2752c | 3067053 | c.-862C>T | upstream_gene_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087476 | c.657C>T | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474144 | p.Trp46Cys | missense_variant | 0.11 |
fprA | 3474165 | c.159C>G | synonymous_variant | 0.12 |
clpC1 | 4038268 | p.Gly813Cys | missense_variant | 0.12 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.17 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.15 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.1 |
clpC1 | 4039829 | p.Leu292Ile | missense_variant | 0.3 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242232 | c.2370T>C | synonymous_variant | 0.36 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245495 | p.Gly755Ser | missense_variant | 0.11 |
embB | 4246787 | p.Pro92Thr | missense_variant | 0.12 |
ethA | 4326176 | p.Glu433Ala | missense_variant | 1.0 |
ethR | 4327631 | p.Ala28Glu | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |