Run ID: ERR4815313
Sample name:
Date: 01-04-2023 13:47:40
Number of reads: 326340
Percentage reads mapped: 86.84
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6146 | p.Thr303Ala | missense_variant | 0.4 |
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 | 491545 | p.Thr255Ala | 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 |
rpoB | 762511 | p.Ala902Val | missense_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764253 | p.Arg295Leu | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776779 | p.Arg568Cys | missense_variant | 0.25 |
mmpS5 | 779612 | c.-709_-708dupAC | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305266 | p.Gly779Asp | missense_variant | 0.15 |
embR | 1416714 | p.Ile212Phe | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474381 | n.724T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476536 | n.2881_2882delAA | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476543 | n.2886G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476567 | n.2910C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1674133 | p.Ile232Val | missense_variant | 0.22 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 0.18 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.2 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.27 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.33 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.22 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.22 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.2 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.2 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.2 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.2 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.18 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156117 | c.-6A>G | upstream_gene_variant | 0.25 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222254 | p.Ile304Thr | missense_variant | 0.2 |
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 | 2518551 | p.Met146Thr | missense_variant | 0.18 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726562 | p.Val124Ile | missense_variant | 0.15 |
folC | 2746406 | p.Phe398Ser | missense_variant | 0.29 |
folC | 2746886 | p.Val238Asp | missense_variant | 0.29 |
pepQ | 2859520 | p.Leu300Pro | missense_variant | 0.33 |
ribD | 2987187 | c.349C>T | synonymous_variant | 1.0 |
Rv2752c | 3067009 | c.-818A>G | upstream_gene_variant | 0.2 |
thyA | 3073729 | p.Val248Glu | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640886 | p.Arg115His | missense_variant | 1.0 |
ddn | 3986997 | p.Thr52Ala | missense_variant | 0.25 |
ddn | 3987121 | p.Lys93Arg | missense_variant | 0.4 |
clpC1 | 4039356 | p.Leu450Gln | missense_variant | 0.25 |
clpC1 | 4039953 | p.Asp251Gly | missense_variant | 0.25 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243911 | p.Leu227Phe | missense_variant | 1.0 |
aftB | 4268074 | p.Ile255Val | missense_variant | 0.67 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |