Run ID: SRR6045744
Sample name:
Date: 04-04-2023 12:04:29
Number of reads: 1013866
Percentage reads mapped: 89.31
Strain: lineage3.1.2
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.33 | 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 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764335 | c.966G>A | synonymous_variant | 0.14 |
rpoC | 764507 | p.Ala380Thr | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473194 | n.1349A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473738 | n.81G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918696 | p.Ala253Pro | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167691 | c.2922C>T | synonymous_variant | 0.11 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168604 | p.Pro670Leu | missense_variant | 1.0 |
PPE35 | 2170349 | p.Thr88Ala | missense_variant | 0.12 |
PPE35 | 2170357 | p.Ala86Thr | missense_variant | 0.14 |
PPE35 | 2170371 | p.Thr81Val | missense_variant | 0.12 |
PPE35 | 2170385 | c.228G>T | synonymous_variant | 0.13 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.15 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.12 |
Rv1979c | 2223257 | c.-93G>C | upstream_gene_variant | 1.0 |
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 | 2518696 | c.582C>T | synonymous_variant | 0.11 |
eis | 2715432 | c.-100C>T | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475052 | p.Asn349Thr | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248241 | c.1728C>G | synonymous_variant | 1.0 |
ethR | 4327693 | p.Asp49Asn | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408147 | p.Ala19Val | missense_variant | 1.0 |