Run ID: ERR245815
Sample name:
Date: 31-03-2023 18:22:45
Number of reads: 2373516
Percentage reads mapped: 99.53
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 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575309 | c.-39C>G | upstream_gene_variant | 0.33 |
mshA | 575932 | p.Glu195Asp | missense_variant | 0.2 |
mshA | 576184 | c.837A>C | synonymous_variant | 0.45 |
ccsA | 620407 | p.Pro173Ala | missense_variant | 0.23 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.41 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.2 |
rpoC | 764905 | p.Phe512Leu | missense_variant | 0.17 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765082 | c.1713G>C | synonymous_variant | 0.23 |
rpoC | 765338 | p.Gln657Glu | missense_variant | 0.21 |
rpoC | 767083 | c.3714C>T | synonymous_variant | 1.0 |
rpoC | 767305 | p.Tyr1312* | stop_gained | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304445 | c.1515G>C | synonymous_variant | 0.25 |
embR | 1417136 | p.Ser71Ile | missense_variant | 0.29 |
embR | 1417233 | c.115C>T | synonymous_variant | 0.3 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473343 | n.1498G>T | non_coding_transcript_exon_variant | 0.28 |
fabG1 | 1673449 | p.Thr4Pro | missense_variant | 0.33 |
fabG1 | 1673546 | p.Ala36Gly | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918377 | c.438T>G | synonymous_variant | 0.2 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.56 |
PPE35 | 2170156 | p.Ala153Pro | missense_variant | 0.75 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714355 | c.978C>G | synonymous_variant | 0.27 |
eis | 2714366 | p.Val323Leu | missense_variant | 0.18 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.43 |
ahpC | 2726756 | c.564C>G | synonymous_variant | 0.22 |
folC | 2746186 | c.1413G>C | synonymous_variant | 0.33 |
folC | 2747263 | c.336C>A | synonymous_variant | 0.16 |
pepQ | 2859381 | c.1038C>G | synonymous_variant | 0.24 |
pepQ | 2859680 | p.Leu247Val | missense_variant | 0.4 |
Rv2752c | 3064741 | p.Gly484Ala | missense_variant | 0.33 |
Rv2752c | 3064836 | p.Leu452Phe | missense_variant | 0.33 |
thyX | 3067531 | p.Ala139Pro | missense_variant | 0.29 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448929 | p.Tyr142* | stop_gained | 0.36 |
Rv3083 | 3449058 | p.Ser185Arg | missense_variant | 0.31 |
Rv3083 | 3449673 | p.Tyr390* | stop_gained | 0.32 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474601 | p.Arg199Gly | missense_variant | 0.26 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
fbiA | 3641271 | p.Tyr243* | stop_gained | 0.5 |
fbiA | 3641534 | p.Ala331Gly | missense_variant | 0.33 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.27 |
fbiB | 3642033 | p.Ala167Pro | missense_variant | 0.29 |
alr | 3840494 | c.927G>C | synonymous_variant | 0.5 |
alr | 3840520 | p.Ala301Pro | missense_variant | 0.31 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
alr | 3840869 | c.552C>G | synonymous_variant | 1.0 |
rpoA | 3878238 | p.Asp90Glu | missense_variant | 0.15 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.25 |
embC | 4239870 | p.Thr3Asn | missense_variant | 0.29 |
embC | 4240646 | p.Phe262Val | missense_variant | 0.2 |
embC | 4241128 | c.1266G>C | synonymous_variant | 0.38 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.44 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.2 |
embA | 4243730 | c.498G>A | synonymous_variant | 0.58 |
embA | 4244375 | c.1143C>G | synonymous_variant | 0.4 |
embA | 4244460 | p.Val410Leu | missense_variant | 0.27 |
embB | 4247284 | c.771G>T | synonymous_variant | 0.11 |
embB | 4248725 | p.Ser738Ala | missense_variant | 0.4 |
ubiA | 4269529 | p.Ala102Gly | missense_variant | 0.4 |
ethA | 4327672 | c.-199G>A | upstream_gene_variant | 0.3 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |