Run ID: SRR21673294
Sample name:
Date: 04-04-2023 02:33:31
Number of reads: 395482
Percentage reads mapped: 99.44
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1918068 | c.130delA | frameshift_variant | 0.14 | capreomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6747 | p.Gln503Arg | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7560 | p.His87Asn | missense_variant | 0.13 |
gyrA | 7761 | p.Pro154Thr | missense_variant | 0.12 |
gyrA | 7859 | c.558A>G | synonymous_variant | 0.22 |
gyrA | 7898 | c.597C>T | synonymous_variant | 0.22 |
gyrA | 7963 | p.Gly221Glu | missense_variant | 0.17 |
gyrA | 9338 | p.Gln679His | missense_variant | 0.15 |
gyrA | 9533 | c.2232C>G | synonymous_variant | 0.12 |
fgd1 | 490877 | p.Met32Thr | missense_variant | 0.15 |
mshA | 575168 | c.-180C>A | upstream_gene_variant | 0.29 |
mshA | 575184 | c.-164G>C | upstream_gene_variant | 0.29 |
mshA | 575857 | c.510G>A | synonymous_variant | 0.14 |
mshA | 576397 | p.Ser350Arg | missense_variant | 0.13 |
ccsA | 620065 | p.Ala59Ser | missense_variant | 0.13 |
ccsA | 620374 | p.Pro162Thr | missense_variant | 0.11 |
rpoB | 760957 | p.Arg384Leu | missense_variant | 0.13 |
rpoB | 761685 | p.Arg627Cys | missense_variant | 0.11 |
rpoB | 762002 | c.2196C>A | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776582 | p.Gln633His | missense_variant | 0.12 |
mmpL5 | 777605 | c.876C>G | synonymous_variant | 0.12 |
mmpL5 | 778036 | p.Val149Ile | missense_variant | 0.13 |
mmpS5 | 778887 | p.Arg7Ser | missense_variant | 0.13 |
mmpR5 | 779123 | p.Val45Glu | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781496 | c.-64G>A | upstream_gene_variant | 0.12 |
rpsL | 781641 | p.Pro28Thr | missense_variant | 0.11 |
rpsL | 781845 | p.Lys96Glu | missense_variant | 0.1 |
rpsL | 781912 | p.Gly118Asp | missense_variant | 0.11 |
rplC | 801066 | c.258G>A | synonymous_variant | 0.13 |
rplC | 801085 | p.Thr93Ser | missense_variant | 0.13 |
fbiC | 1303200 | c.270G>T | synonymous_variant | 0.17 |
fbiC | 1304128 | p.Gln400* | stop_gained | 0.12 |
fbiC | 1304517 | c.1587C>G | synonymous_variant | 0.17 |
Rv1258c | 1406878 | c.462delT | frameshift_variant | 0.13 |
Rv1258c | 1406909 | c.432C>A | synonymous_variant | 0.2 |
Rv1258c | 1407308 | c.33G>A | synonymous_variant | 0.17 |
Rv1258c | 1407506 | c.-167dupG | upstream_gene_variant | 0.2 |
embR | 1416982 | c.366C>A | synonymous_variant | 0.14 |
embR | 1417460 | c.-113G>A | upstream_gene_variant | 0.14 |
atpE | 1460915 | c.-130C>A | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673233 | c.-207T>G | upstream_gene_variant | 1.0 |
fabG1 | 1673237 | c.-203C>A | upstream_gene_variant | 0.17 |
fabG1 | 1673871 | p.Ser144Arg | missense_variant | 0.11 |
rpsA | 1833483 | c.-59G>T | upstream_gene_variant | 0.12 |
tlyA | 1917869 | c.-71A>G | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918372 | p.Gly145Cys | missense_variant | 0.22 |
tlyA | 1918441 | p.Val168Phe | missense_variant | 0.12 |
ndh | 2101757 | p.Leu429Arg | missense_variant | 0.13 |
ndh | 2101876 | c.1167C>A | synonymous_variant | 0.11 |
katG | 2153916 | p.Met732Ile | missense_variant | 0.11 |
katG | 2154790 | p.Pro441Gln | missense_variant | 0.17 |
katG | 2155302 | c.810C>T | synonymous_variant | 0.29 |
katG | 2156123 | c.-12G>C | upstream_gene_variant | 0.11 |
PPE35 | 2168139 | p.Ala825Asp | missense_variant | 0.2 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169580 | p.Gly345Ser | missense_variant | 0.14 |
PPE35 | 2170365 | p.Ala83Val | missense_variant | 0.33 |
Rv1979c | 2222143 | p.Ser341* | stop_gained | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288742 | p.Thr167Ile | missense_variant | 0.14 |
pncA | 2289734 | c.-493C>A | upstream_gene_variant | 0.15 |
kasA | 2518129 | c.15C>T | synonymous_variant | 0.22 |
kasA | 2518433 | c.319C>A | synonymous_variant | 0.15 |
kasA | 2518635 | p.Gly174Val | missense_variant | 0.2 |
kasA | 2518819 | p.Asp235Glu | missense_variant | 0.22 |
eis | 2714543 | c.790C>A | synonymous_variant | 0.22 |
eis | 2715161 | p.Val58Leu | missense_variant | 0.12 |
ahpC | 2726735 | c.543C>G | synonymous_variant | 0.12 |
folC | 2746647 | p.Gln318Lys | missense_variant | 0.25 |
folC | 2746976 | p.Asp208Val | missense_variant | 0.15 |
folC | 2746982 | p.Gly206Val | missense_variant | 0.13 |
folC | 2747483 | p.Pro39Leu | missense_variant | 0.17 |
pepQ | 2859569 | p.Ala284Ser | missense_variant | 0.17 |
pepQ | 2859617 | p.Ala268Thr | missense_variant | 0.17 |
pepQ | 2859768 | p.Phe217Leu | missense_variant | 0.13 |
pepQ | 2860143 | c.276G>T | synonymous_variant | 0.15 |
pepQ | 2860199 | p.Ala74Ser | missense_variant | 0.12 |
ribD | 2986818 | c.-21C>A | upstream_gene_variant | 0.14 |
ribD | 2987284 | p.Ala149Asp | missense_variant | 0.11 |
Rv2752c | 3064967 | p.Leu409Met | missense_variant | 0.11 |
Rv2752c | 3065535 | c.657C>G | synonymous_variant | 0.14 |
Rv2752c | 3065938 | p.Asp85Val | missense_variant | 0.13 |
Rv2752c | 3066082 | p.Leu37Pro | missense_variant | 0.11 |
Rv2752c | 3066176 | p.Pro6Ser | missense_variant | 0.14 |
Rv2752c | 3066355 | c.-164T>C | upstream_gene_variant | 0.15 |
thyX | 3067480 | p.Asp156Asn | missense_variant | 0.15 |
thyX | 3067624 | p.Tyr108His | missense_variant | 0.12 |
thyX | 3067820 | c.126C>A | synonymous_variant | 0.14 |
thyX | 3068124 | c.-179G>A | upstream_gene_variant | 0.13 |
thyA | 3074295 | c.177G>T | synonymous_variant | 0.2 |
thyA | 3074445 | c.27C>A | synonymous_variant | 0.12 |
ald | 3087087 | p.Ile90Phe | missense_variant | 0.13 |
fbiD | 3339355 | c.238C>T | synonymous_variant | 0.2 |
fbiD | 3339395 | p.Asn93Ser | missense_variant | 0.18 |
fbiD | 3339491 | p.Leu125Pro | missense_variant | 0.13 |
fbiD | 3339587 | p.Ala157Glu | missense_variant | 0.13 |
fprA | 3473825 | c.-182T>C | upstream_gene_variant | 0.1 |
fprA | 3473837 | c.-169delG | upstream_gene_variant | 0.13 |
fprA | 3474174 | c.168T>C | synonymous_variant | 0.13 |
fprA | 3475375 | c.1369T>C | stop_lost&splice_region_variant | 0.17 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 0.12 |
whiB7 | 3568534 | p.Arg49Met | missense_variant | 0.1 |
Rv3236c | 3613065 | c.50_51delTG | frameshift_variant | 0.11 |
fbiA | 3640616 | c.77delG | frameshift_variant | 0.12 |
fbiA | 3641163 | p.Asp207Glu | missense_variant | 0.11 |
fbiB | 3641738 | p.Glu68Asp | missense_variant | 0.11 |
fbiB | 3641953 | p.Leu140Arg | missense_variant | 0.13 |
rpoA | 3877688 | p.Glu274* | stop_gained | 0.12 |
rpoA | 3877913 | p.Lys199* | stop_gained | 0.13 |
clpC1 | 4038650 | c.2055C>A | synonymous_variant | 0.12 |
clpC1 | 4038747 | p.Arg653Leu | missense_variant | 0.18 |
clpC1 | 4039340 | p.Lys455Asn | missense_variant | 0.17 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 1.0 |
embC | 4241357 | p.Ala499Thr | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244162 | c.930G>A | synonymous_variant | 0.25 |
embA | 4244551 | p.Ala440Asp | missense_variant | 0.13 |
embA | 4244685 | p.Ile485Phe | missense_variant | 0.17 |
embB | 4246665 | p.Gln51Leu | missense_variant | 0.11 |
embB | 4247055 | p.Leu181Arg | missense_variant | 0.12 |
embB | 4247093 | p.Gly194Trp | missense_variant | 0.17 |
embB | 4247525 | p.Ala338Ser | missense_variant | 0.13 |
embB | 4248075 | p.Glu521Val | missense_variant | 0.11 |
embB | 4249401 | p.Val963Ala | missense_variant | 0.2 |
embB | 4249519 | c.3006C>T | synonymous_variant | 0.17 |
aftB | 4267061 | p.Leu592Phe | missense_variant | 0.14 |
aftB | 4267294 | p.Ala515Ser | missense_variant | 0.14 |
aftB | 4267698 | p.Leu380Pro | missense_variant | 0.11 |
ubiA | 4269238 | p.Ala199Asp | missense_variant | 0.15 |
ethA | 4326068 | p.Arg469Leu | missense_variant | 0.11 |
ethA | 4326830 | p.Gln215Arg | missense_variant | 0.13 |
ethA | 4328269 | c.-796C>T | upstream_gene_variant | 0.12 |
ethA | 4328331 | c.-858C>A | upstream_gene_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408365 | c.-163C>A | upstream_gene_variant | 0.11 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |