Run ID: ERR176675
Sample name:
Date: 31-03-2023 15:09:30
Number of reads: 2934919
Percentage reads mapped: 88.89
Strain: lineage4.3.4.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 0.98 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 0.95 |
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 | 490751 | c.-32T>G | upstream_gene_variant | 0.25 |
ccsA | 620748 | c.858T>C | synonymous_variant | 0.13 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.14 |
ccsA | 620781 | c.891C>G | synonymous_variant | 0.14 |
ccsA | 620783 | p.Ala298Val | missense_variant | 0.14 |
ccsA | 620787 | c.897C>A | synonymous_variant | 0.14 |
ccsA | 620796 | c.906C>G | synonymous_variant | 0.14 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.13 |
rpoB | 760649 | c.843G>C | synonymous_variant | 0.13 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.12 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.12 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.12 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.12 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.12 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.13 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.15 |
rpoB | 760982 | c.1176G>T | synonymous_variant | 0.14 |
rpoB | 760985 | c.1179G>T | synonymous_variant | 0.14 |
rpoB | 760991 | c.1185G>T | synonymous_variant | 0.13 |
rpoB | 761006 | c.1200C>T | synonymous_variant | 0.18 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.16 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.2 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.21 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.17 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.17 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.16 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.15 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.15 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.15 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.16 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.14 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.14 |
rpoB | 761189 | c.1383T>G | synonymous_variant | 0.13 |
rpoB | 761240 | c.1434C>T | synonymous_variant | 0.12 |
rpoB | 761435 | c.1629T>C | synonymous_variant | 0.15 |
rpoB | 761438 | c.1632G>C | synonymous_variant | 0.15 |
rpoB | 761444 | c.1638T>C | synonymous_variant | 0.15 |
rpoB | 761452 | p.Val549Asp | missense_variant | 0.13 |
rpoB | 761457 | p.Pro551Ser | missense_variant | 0.13 |
rpoB | 761465 | c.1659G>A | synonymous_variant | 0.16 |
rpoB | 761471 | c.1665C>T | synonymous_variant | 0.17 |
rpoB | 761477 | c.1671C>T | synonymous_variant | 0.18 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.16 |
rpoB | 761495 | c.1689G>A | synonymous_variant | 0.16 |
rpoB | 761504 | c.1698C>G | synonymous_variant | 0.17 |
rpoB | 761510 | c.1704T>C | synonymous_variant | 0.18 |
rpoB | 761531 | c.1725C>G | synonymous_variant | 0.13 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.13 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.11 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.12 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.13 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.13 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.16 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.18 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.13 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.16 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.15 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.15 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.12 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.12 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.12 |
rpoC | 763726 | c.357C>T | synonymous_variant | 0.12 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.12 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.13 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.13 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.12 |
rpoC | 763771 | c.402C>T | synonymous_variant | 0.13 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.96 |
rpoC | 765934 | c.2565C>T | synonymous_variant | 0.14 |
rpoC | 766309 | c.2940G>A | synonymous_variant | 0.13 |
rpoC | 766315 | c.2946C>G | synonymous_variant | 0.13 |
rpoC | 766321 | c.2952C>G | synonymous_variant | 0.12 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.13 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 0.14 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.13 |
rpoC | 766996 | c.3627C>G | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303674 | c.744C>G | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1833613 | c.72C>A | synonymous_variant | 0.16 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.16 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.15 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.15 |
rpsA | 1833703 | c.162C>T | synonymous_variant | 0.14 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.13 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.13 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.14 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.14 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.14 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.14 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.12 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.12 |
rpsA | 1833859 | c.318C>T | synonymous_variant | 0.13 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.13 |
rpsA | 1833895 | c.354G>C | synonymous_variant | 0.15 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.12 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.12 |
rpsA | 1834231 | c.690T>G | synonymous_variant | 0.13 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.18 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.22 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.21 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.21 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.19 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.19 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.21 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.18 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.12 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.16 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.15 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.16 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.15 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.14 |
rpsA | 1834477 | c.936C>T | synonymous_variant | 0.16 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.12 |
rpsA | 1834519 | c.978G>C | synonymous_variant | 0.13 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.2 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.19 |
rpsA | 1834603 | c.1062G>A | synonymous_variant | 0.2 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.21 |
rpsA | 1834612 | c.1071G>A | synonymous_variant | 0.21 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.16 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.95 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.99 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
rpoA | 3877557 | c.951C>G | synonymous_variant | 0.12 |
rpoA | 3877587 | c.921A>C | synonymous_variant | 0.12 |
rpoA | 3877900 | p.Ser203Thr | missense_variant | 0.12 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.12 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.13 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.12 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.12 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.14 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.14 |
rpoA | 3878418 | c.90C>T | synonymous_variant | 0.14 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.15 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038425 | c.2280C>A | synonymous_variant | 0.15 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 0.18 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 0.19 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 0.23 |
clpC1 | 4038486 | p.Gly740Asn | missense_variant | 0.19 |
clpC1 | 4038491 | c.2214C>T | synonymous_variant | 0.19 |
clpC1 | 4038502 | p.Ile735Val | missense_variant | 0.24 |
clpC1 | 4038508 | c.2197C>T | synonymous_variant | 0.25 |
clpC1 | 4038518 | c.2187G>T | synonymous_variant | 0.22 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.19 |
clpC1 | 4038537 | p.Thr723Ser | missense_variant | 0.18 |
clpC1 | 4038539 | c.2166G>C | synonymous_variant | 0.18 |
clpC1 | 4038569 | c.2136C>T | synonymous_variant | 0.15 |
clpC1 | 4038575 | c.2130C>G | synonymous_variant | 0.15 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.23 |
clpC1 | 4038875 | c.1830C>G | synonymous_variant | 0.11 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.12 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.15 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.16 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.16 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.15 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.2 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.18 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.2 |
clpC1 | 4039025 | c.1680C>G | synonymous_variant | 0.19 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 0.15 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.16 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.12 |
clpC1 | 4039339 | p.Thr456Pro | missense_variant | 0.12 |
clpC1 | 4039361 | c.1344C>A | synonymous_variant | 0.14 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.15 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.12 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.35 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.13 |
clpC1 | 4040000 | c.705C>T | synonymous_variant | 0.17 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.15 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.12 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.14 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.14 |
clpC1 | 4040309 | c.396C>T | synonymous_variant | 0.13 |
panD | 4044225 | c.57C>T | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.99 |