Run ID: SRR18910985
Sample name:
Date: 03-04-2023 20:39:53
Number of reads: 222099
Percentage reads mapped: 99.29
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8151 | p.Ile284Val | missense_variant | 0.2 |
gyrA | 8271 | p.Ala324Thr | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490707 | c.-76G>T | upstream_gene_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575376 | p.Ser10* | stop_gained | 0.13 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.75 |
ccsA | 619937 | p.Trp16* | stop_gained | 0.13 |
rpoB | 760352 | p.Asp182Glu | missense_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765793 | c.2424C>A | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775792 | p.Val897Phe | missense_variant | 0.11 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800744 | c.-65G>T | upstream_gene_variant | 0.22 |
fbiC | 1303873 | p.Leu315Met | missense_variant | 0.12 |
embR | 1416880 | p.Phe156Leu | missense_variant | 1.0 |
embR | 1417442 | c.-95C>A | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471673 | n.-173C>T | upstream_gene_variant | 0.17 |
rrl | 1475513 | n.1856T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475675 | n.2018A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 0.15 |
fabG1 | 1673681 | p.Pro81Gln | missense_variant | 0.15 |
fabG1 | 1674101 | p.Val221Asp | missense_variant | 0.13 |
inhA | 1674772 | p.Ala191Thr | missense_variant | 0.67 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834186 | c.645C>G | synonymous_variant | 0.17 |
rpsA | 1834907 | p.Ser456Pro | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918072 | p.Ala45Thr | missense_variant | 0.15 |
ndh | 2102267 | p.Val259Gly | missense_variant | 0.13 |
katG | 2154579 | p.Asp511Glu | missense_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156501 | c.-390C>T | upstream_gene_variant | 0.17 |
katG | 2156530 | c.-419G>A | upstream_gene_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169775 | p.Ala280Thr | missense_variant | 0.5 |
PPE35 | 2170349 | p.Thr88Ala | missense_variant | 0.13 |
PPE35 | 2170357 | p.Ala86Thr | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714278 | p.Asp352Gly | missense_variant | 0.2 |
eis | 2715328 | p.Thr2Asn | missense_variant | 0.15 |
ahpC | 2726669 | p.Asp159Glu | missense_variant | 0.2 |
pepQ | 2859700 | p.Gly240Ala | missense_variant | 0.67 |
ribD | 2986915 | p.Gly26Val | missense_variant | 0.12 |
ribD | 2986945 | p.Asp36Gly | missense_variant | 0.11 |
Rv2752c | 3064794 | c.1398C>T | synonymous_variant | 0.14 |
Rv2752c | 3065227 | c.964delG | frameshift_variant | 0.14 |
thyA | 3074199 | c.273G>A | synonymous_variant | 0.2 |
thyA | 3074258 | c.214C>T | synonymous_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087504 | p.Val229Ile | missense_variant | 0.22 |
ald | 3087530 | c.711G>T | synonymous_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613170 | c.-54G>A | upstream_gene_variant | 0.25 |
fbiA | 3641522 | p.Ala327Val | missense_variant | 0.13 |
fbiB | 3641590 | p.Gly19Val | missense_variant | 0.13 |
rpoA | 3877899 | c.609C>T | synonymous_variant | 0.2 |
ddn | 3987144 | p.Gln101Lys | missense_variant | 0.12 |
ddn | 3987242 | p.Tyr133* | stop_gained | 0.12 |
clpC1 | 4038467 | c.2238C>T | synonymous_variant | 0.14 |
clpC1 | 4039230 | p.Thr492Asn | missense_variant | 0.17 |
clpC1 | 4039307 | c.1397delA | frameshift_variant | 0.29 |
embC | 4240214 | p.Asp118Asn | missense_variant | 0.18 |
embC | 4240546 | c.684G>A | synonymous_variant | 0.2 |
embA | 4242577 | c.-656A>G | upstream_gene_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242756 | p.Ile965Asn | missense_variant | 0.11 |
embA | 4242994 | c.-239G>T | upstream_gene_variant | 0.12 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245847 | p.Ser872Phe | missense_variant | 0.5 |
embA | 4246351 | p.Ser1040* | stop_gained | 0.2 |
embB | 4247040 | c.531dupC | frameshift_variant | 0.18 |
aftB | 4267051 | p.Glu596Lys | missense_variant | 0.25 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267731 | p.Arg369Leu | missense_variant | 0.22 |
ethA | 4326311 | p.Asn388Thr | missense_variant | 0.1 |
whiB6 | 4338286 | p.Val79Asp | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407916 | p.Arg96Leu | missense_variant | 0.11 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408398 | c.-196C>T | upstream_gene_variant | 0.13 |