Run ID: SRR4035748
Sample name:
Date: 04-04-2023 07:16:30
Number of reads: 1150350
Percentage reads mapped: 99.55
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 |
---|---|---|---|---|
gyrB | 6371 | p.Thr378Ala | missense_variant | 0.13 |
gyrA | 7000 | c.-302C>T | upstream_gene_variant | 0.13 |
gyrB | 7025 | p.Lys596Glu | missense_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7672 | p.Pro124Gln | missense_variant | 0.13 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
fgd1 | 491729 | p.Asp316Gly | missense_variant | 0.11 |
mshA | 575636 | p.Asp97Asn | missense_variant | 0.12 |
mshA | 576275 | p.Asp310Asn | missense_variant | 0.12 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760608 | c.802C>T | synonymous_variant | 0.15 |
rpoB | 760669 | p.Thr288Met | missense_variant | 0.15 |
rpoB | 760721 | c.915C>T | synonymous_variant | 0.12 |
rpoB | 760732 | p.Lys309Arg | missense_variant | 0.12 |
rpoB | 761424 | p.Ser540Pro | missense_variant | 0.15 |
rpoB | 761444 | c.1638T>G | synonymous_variant | 0.15 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776651 | c.1830C>T | synonymous_variant | 0.13 |
mmpL5 | 776663 | c.1818C>T | synonymous_variant | 0.14 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473316 | n.1473delG | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473454 | n.-204A>T | upstream_gene_variant | 0.25 |
rrl | 1476478 | n.2821G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476520 | n.2863G>A | non_coding_transcript_exon_variant | 0.18 |
rpsA | 1834237 | c.696C>T | synonymous_variant | 0.2 |
rpsA | 1834265 | p.Trp242Arg | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101975 | c.1067delC | frameshift_variant | 0.12 |
ndh | 2102762 | p.Leu94Pro | missense_variant | 0.12 |
ndh | 2102771 | c.271delC | frameshift_variant | 0.17 |
katG | 2154332 | p.Phe594Leu | missense_variant | 0.2 |
katG | 2156013 | c.99C>A | synonymous_variant | 0.14 |
katG | 2156049 | c.63C>G | synonymous_variant | 0.11 |
PPE35 | 2168372 | c.2241G>A | synonymous_variant | 0.13 |
PPE35 | 2168713 | p.Ala634Pro | missense_variant | 0.12 |
PPE35 | 2169119 | c.1493delT | frameshift_variant | 0.18 |
PPE35 | 2170158 | p.Ala152Gly | missense_variant | 0.11 |
Rv1979c | 2222927 | p.Ala80Thr | missense_variant | 0.2 |
Rv1979c | 2223270 | c.-106C>G | upstream_gene_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290152 | c.-911G>A | upstream_gene_variant | 0.14 |
kasA | 2517934 | c.-181A>T | upstream_gene_variant | 0.12 |
kasA | 2517941 | c.-174C>T | upstream_gene_variant | 0.12 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ahpC | 2726210 | c.18T>C | synonymous_variant | 0.2 |
ahpC | 2726263 | p.Ser24Phe | missense_variant | 0.13 |
ahpC | 2726331 | p.Trp47Arg | missense_variant | 0.25 |
thyX | 3067918 | p.Gln10* | stop_gained | 0.18 |
thyX | 3067932 | p.Ala5Val | missense_variant | 0.14 |
thyX | 3068125 | c.-180G>T | upstream_gene_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449456 | p.Thr318Asn | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474076 | p.Lys24Glu | missense_variant | 0.12 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
Rv3236c | 3612329 | p.Leu263Pro | missense_variant | 0.15 |
fbiA | 3640628 | p.Ala29Asp | missense_variant | 0.2 |
fbiB | 3642691 | p.Val386Asp | missense_variant | 0.17 |
panD | 4044312 | c.-32delC | upstream_gene_variant | 0.18 |
embC | 4241378 | p.Val506Ile | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embC | 4242944 | p.Asn1028Asp | missense_variant | 0.11 |
embA | 4244199 | p.Trp323Arg | missense_variant | 0.11 |
embB | 4245527 | c.-987C>T | upstream_gene_variant | 0.13 |
embB | 4246521 | p.Gln3Pro | missense_variant | 0.11 |
embB | 4248751 | c.2238C>G | synonymous_variant | 0.22 |
embB | 4249527 | p.Gly1005Asp | missense_variant | 0.12 |
embB | 4249715 | p.Asp1068His | missense_variant | 0.12 |
embB | 4249723 | c.3210G>C | synonymous_variant | 0.1 |
ethA | 4326471 | p.Ala335Ser | missense_variant | 0.17 |
ethA | 4326638 | p.Arg279Gln | missense_variant | 0.15 |
ethA | 4327546 | c.-74delC | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |