Run ID: SRR18213740
Sample name:
Date: 03-04-2023 19:27:18
Number of reads: 363173
Percentage reads mapped: 84.67
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 |
---|---|---|---|---|
gyrA | 6922 | c.-380G>T | upstream_gene_variant | 0.2 |
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 | 9381 | p.Gly694Arg | missense_variant | 1.0 |
fgd1 | 491501 | p.Glu240Gly | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576253 | c.906G>A | synonymous_variant | 0.25 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761719 | p.Ala638Gly | missense_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762521 | c.-849C>G | upstream_gene_variant | 0.13 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.12 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.12 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.12 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.15 |
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 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407084 | p.Val86Gly | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834634 | p.Ala365Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154519 | c.1593G>A | synonymous_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.18 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.17 |
Rv1979c | 2222359 | c.805delC | frameshift_variant | 0.12 |
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 |
eis | 2714628 | c.705A>G | synonymous_variant | 0.14 |
eis | 2714647 | c.685delG | frameshift_variant | 0.17 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087808 | p.Arg330Gln | missense_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612835 | c.282T>G | synonymous_variant | 0.4 |
rpoA | 3877510 | p.Glu333Ala | missense_variant | 1.0 |
rpoA | 3878648 | c.-141C>T | upstream_gene_variant | 1.0 |
panD | 4044028 | c.253delG | frameshift_variant | 0.18 |
embC | 4241666 | p.Ala602Thr | missense_variant | 0.2 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245111 | p.Val627Ile | missense_variant | 0.2 |
embB | 4246166 | c.-348G>A | upstream_gene_variant | 1.0 |
embB | 4248246 | p.Ile578Asn | missense_variant | 0.15 |
ethA | 4326905 | p.Leu190Pro | missense_variant | 0.38 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |