Run ID: SRR4035711
Sample name:
Date: 04-04-2023 07:15:06
Number of reads: 947431
Percentage reads mapped: 99.46
Strain: lineage4.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7495 | p.Arg65Pro | missense_variant | 0.18 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7971 | p.Lys224* | stop_gained | 0.14 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 8360 | c.1059G>A | synonymous_variant | 0.13 |
gyrA | 8707 | p.Leu469Pro | missense_variant | 0.14 |
gyrA | 8759 | c.1458C>T | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9360 | p.Asp687His | missense_variant | 0.15 |
gyrA | 9474 | p.Val725Met | missense_variant | 0.12 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
ccsA | 620853 | c.963G>C | synonymous_variant | 0.18 |
ccsA | 620860 | p.Gly324Arg | missense_variant | 0.23 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761214 | p.His470Asp | missense_variant | 0.12 |
rpoB | 761453 | c.1647C>G | synonymous_variant | 0.18 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 764418 | p.Arg350His | missense_variant | 0.23 |
rpoC | 764834 | p.Glu489Lys | missense_variant | 0.13 |
rpoC | 764846 | p.Glu493Lys | missense_variant | 0.17 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765682 | c.2313C>T | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
mmpL5 | 777723 | p.His253Leu | missense_variant | 0.13 |
mmpR5 | 778475 | c.-515G>A | upstream_gene_variant | 0.13 |
mmpL5 | 779112 | c.-632G>A | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801015 | p.Gln69His | missense_variant | 0.13 |
rplC | 801031 | p.Val75Ile | missense_variant | 0.12 |
fbiC | 1302837 | c.-94G>C | upstream_gene_variant | 0.11 |
fbiC | 1303055 | p.Asp42Gly | missense_variant | 0.11 |
fbiC | 1303604 | p.Thr225Ile | missense_variant | 0.12 |
Rv1258c | 1406326 | p.Arg339Gly | missense_variant | 0.18 |
Rv1258c | 1406470 | p.Met291Val | missense_variant | 0.15 |
Rv1258c | 1406519 | c.822A>G | synonymous_variant | 0.12 |
Rv1258c | 1407466 | c.-127delC | upstream_gene_variant | 0.18 |
embR | 1417037 | p.Ser104Asn | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472335 | n.490A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472687 | n.842A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473641 | n.-17T>C | upstream_gene_variant | 0.13 |
rrl | 1475457 | n.1800G>C | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673173 | c.-267G>C | upstream_gene_variant | 0.11 |
inhA | 1674380 | p.Leu60Pro | missense_variant | 0.12 |
inhA | 1674992 | p.Ala264Gly | missense_variant | 0.15 |
rpsA | 1833862 | c.321G>A | synonymous_variant | 0.29 |
rpsA | 1834874 | p.Ala445Pro | missense_variant | 0.12 |
tlyA | 1917963 | c.24C>T | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918499 | p.Val187Glu | missense_variant | 0.15 |
ndh | 2101803 | p.Leu414Met | missense_variant | 0.13 |
ndh | 2102708 | p.Tyr112Cys | missense_variant | 0.11 |
ndh | 2102801 | p.Asn81Thr | missense_variant | 0.17 |
ndh | 2102808 | p.Gln79* | stop_gained | 0.17 |
ndh | 2102814 | p.Arg77Gly | missense_variant | 0.17 |
ndh | 2102828 | p.Thr72Ile | missense_variant | 0.15 |
ndh | 2103224 | c.-183A>G | upstream_gene_variant | 0.14 |
katG | 2153933 | p.Ala727Ser | missense_variant | 0.25 |
katG | 2154339 | c.1773A>G | synonymous_variant | 0.15 |
katG | 2154985 | p.Thr376Met | missense_variant | 0.2 |
katG | 2156523 | c.-412G>A | upstream_gene_variant | 0.15 |
PPE35 | 2169014 | c.1599G>A | synonymous_variant | 0.18 |
PPE35 | 2169545 | p.His356Gln | missense_variant | 0.18 |
PPE35 | 2170069 | p.Pro182Ser | missense_variant | 0.2 |
Rv1979c | 2222826 | c.338delT | frameshift_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289373 | c.-132A>G | upstream_gene_variant | 0.12 |
kasA | 2517925 | c.-189delG | upstream_gene_variant | 0.14 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714722 | p.Cys204Ser | missense_variant | 0.13 |
eis | 2715034 | p.Met100Lys | missense_variant | 0.14 |
ahpC | 2725915 | c.-278C>T | upstream_gene_variant | 0.15 |
folC | 2747148 | p.Lys151Glu | missense_variant | 0.11 |
pepQ | 2859931 | p.Leu163Arg | missense_variant | 0.13 |
pepQ | 2860480 | c.-62G>A | upstream_gene_variant | 0.13 |
Rv2752c | 3065940 | c.251delA | frameshift_variant | 0.12 |
Rv2752c | 3067098 | c.-907A>G | upstream_gene_variant | 0.12 |
thyX | 3067542 | p.Ala135Val | missense_variant | 0.25 |
thyX | 3068128 | c.-183C>T | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087690 | p.His291Tyr | missense_variant | 0.18 |
ald | 3087723 | p.Pro302Ala | missense_variant | 0.15 |
Rv3083 | 3448838 | p.Arg112Gln | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474400 | p.Tyr132His | missense_variant | 0.1 |
fprA | 3475230 | c.1224C>T | synonymous_variant | 0.14 |
fprA | 3475236 | c.1230A>G | synonymous_variant | 0.12 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
Rv3236c | 3611981 | p.Ala379Gly | missense_variant | 0.15 |
Rv3236c | 3611999 | p.Thr373Ile | missense_variant | 0.15 |
Rv3236c | 3612449 | p.Leu223Arg | missense_variant | 0.13 |
Rv3236c | 3612509 | p.Gly203Asp | missense_variant | 0.18 |
Rv3236c | 3612922 | c.195T>C | synonymous_variant | 0.12 |
Rv3236c | 3612933 | p.Ala62Thr | missense_variant | 0.13 |
fbiA | 3640430 | c.-113A>T | upstream_gene_variant | 0.12 |
fbiB | 3642601 | p.Gly356Ala | missense_variant | 0.11 |
alr | 3840554 | c.867G>A | synonymous_variant | 0.12 |
alr | 3841031 | c.390C>A | synonymous_variant | 0.14 |
alr | 3841115 | c.306T>C | synonymous_variant | 0.2 |
rpoA | 3877851 | p.Phe219Leu | missense_variant | 0.14 |
rpoA | 3878442 | c.66G>A | synonymous_variant | 0.13 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.3 |
clpC1 | 4038624 | p.Lys694Ile | missense_variant | 0.14 |
clpC1 | 4039318 | p.Glu463Lys | missense_variant | 0.15 |
clpC1 | 4040085 | p.Arg207His | missense_variant | 0.22 |
embC | 4240777 | c.915G>A | synonymous_variant | 0.14 |
embC | 4241847 | p.Thr662Ser | missense_variant | 0.12 |
embA | 4242340 | c.-893C>A | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243123 | c.-110T>C | upstream_gene_variant | 0.17 |
embA | 4243976 | p.Phe248Leu | missense_variant | 0.14 |
embA | 4243994 | c.762C>T | synonymous_variant | 0.15 |
embA | 4244201 | p.Trp323* | stop_gained | 0.14 |
embA | 4244226 | p.Gly332* | stop_gained | 0.14 |
embA | 4244262 | c.1030C>T | synonymous_variant | 0.18 |
embA | 4245357 | p.Ala709Thr | missense_variant | 0.14 |
embB | 4245761 | c.-753C>T | upstream_gene_variant | 0.2 |
embA | 4246236 | p.Leu1002Val | missense_variant | 0.11 |
embB | 4246655 | p.Pro48Ser | missense_variant | 0.2 |
embB | 4246864 | c.351C>G | synonymous_variant | 0.13 |
embB | 4247081 | p.Thr190Ser | missense_variant | 0.15 |
embB | 4247413 | p.Asp300Glu | missense_variant | 0.12 |
embB | 4249132 | c.2619G>A | synonymous_variant | 0.17 |
embB | 4249523 | p.Asn1004Tyr | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407961 | p.Ile81Thr | missense_variant | 0.11 |