Run ID: SRR11972231
Sample name:
Date: 03-04-2023 05:32:43
Number of reads: 368124
Percentage reads mapped: 98.15
Strain: lineage3.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1.2 | East-African-Indian | CAS;CAS2 | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6173 | p.Glu312Gln | missense_variant | 0.25 |
gyrB | 6372 | p.Thr378Ser | missense_variant | 1.0 |
gyrB | 6546 | p.Gly436Asp | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7484 | p.Asp61Glu | missense_variant | 0.29 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7588 | p.Leu96Gln | missense_variant | 0.2 |
gyrA | 8267 | c.966G>A | synonymous_variant | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9505 | p.Thr735Ile | missense_variant | 0.29 |
gyrA | 9567 | p.Asp756Asn | missense_variant | 0.14 |
fgd1 | 490915 | p.Arg45Cys | missense_variant | 0.25 |
fgd1 | 490952 | p.Trp57Leu | missense_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760761 | p.Gly319Ser | missense_variant | 0.25 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763107 | p.Val1101Ile | missense_variant | 0.12 |
rpoC | 766509 | p.Ala1047Gly | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778606 | c.-126C>T | upstream_gene_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781416 | c.-144C>T | upstream_gene_variant | 0.18 |
rplC | 800959 | p.Gln51* | stop_gained | 0.11 |
rplC | 801085 | p.Thr93Ser | missense_variant | 0.12 |
fbiC | 1303928 | p.Ala333Val | missense_variant | 1.0 |
Rv1258c | 1406556 | p.Trp262Leu | missense_variant | 0.12 |
embR | 1417330 | c.18A>C | synonymous_variant | 0.92 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673638 | p.Ala67Thr | missense_variant | 0.5 |
inhA | 1674591 | p.Met130Ile | missense_variant | 0.33 |
tlyA | 1917757 | c.-183T>A | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918065 | c.126G>A | synonymous_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156377 | c.-266C>T | upstream_gene_variant | 0.17 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168604 | p.Pro670Leu | missense_variant | 1.0 |
PPE35 | 2168799 | p.Phe605Cys | missense_variant | 0.14 |
PPE35 | 2169266 | c.1347C>T | synonymous_variant | 0.15 |
PPE35 | 2169939 | p.Gly225Ala | missense_variant | 0.12 |
PPE35 | 2169941 | c.672C>T | synonymous_variant | 0.12 |
PPE35 | 2169944 | c.669G>C | synonymous_variant | 0.11 |
PPE35 | 2169947 | c.666T>C | synonymous_variant | 0.11 |
PPE35 | 2170031 | c.582C>T | synonymous_variant | 0.14 |
Rv1979c | 2222663 | p.Val168Leu | missense_variant | 0.14 |
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 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3065609 | p.Gly195Arg | missense_variant | 0.12 |
Rv2752c | 3066312 | c.-121C>G | upstream_gene_variant | 0.11 |
thyX | 3067728 | p.Leu73Gln | missense_variant | 0.12 |
thyA | 3073692 | c.780A>G | synonymous_variant | 0.12 |
thyA | 3074023 | p.Phe150Cys | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473909 | c.-98G>A | upstream_gene_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474462 | c.456T>C | synonymous_variant | 0.33 |
Rv3236c | 3613214 | c.-98C>T | upstream_gene_variant | 0.12 |
fbiA | 3640539 | c.-4C>T | upstream_gene_variant | 0.13 |
fbiB | 3641820 | p.Glu96Lys | missense_variant | 0.17 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.1 |
panD | 4044002 | p.Asp94Asn | missense_variant | 0.11 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242897 | p.Leu1012Pro | missense_variant | 0.2 |
embA | 4244584 | p.Gly451Glu | missense_variant | 1.0 |
embB | 4249278 | c.2766delC | frameshift_variant | 0.22 |
aftB | 4267209 | p.Trp543* | stop_gained | 0.18 |
aftB | 4268314 | c.523T>C | synonymous_variant | 1.0 |
ethA | 4328220 | c.-747G>A | upstream_gene_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407610 | p.Pro198Leu | missense_variant | 0.33 |