Run ID: SRR21735254
Sample name:
Date: 04-04-2023 03:22:49
Number of reads: 827235
Percentage reads mapped: 99.33
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5602 | c.363C>T | synonymous_variant | 0.22 |
gyrB | 5845 | p.Lys202Asn | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Arg | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8628 | c.1327C>T | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.11 |
fgd1 | 491570 | p.Asp263Gly | missense_variant | 0.11 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575279 | c.-69C>T | upstream_gene_variant | 0.11 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 619818 | c.-73G>A | upstream_gene_variant | 0.18 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761319 | p.Phe505Leu | missense_variant | 0.15 |
rpoB | 762612 | p.Ser936Gly | missense_variant | 0.11 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766365 | p.Ala999Val | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777439 | p.Ala348Thr | missense_variant | 0.11 |
mmpL5 | 777979 | p.Ala168Ser | missense_variant | 1.0 |
mmpL5 | 778045 | p.Ala146Thr | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801440 | p.Ala211Val | missense_variant | 0.12 |
fbiC | 1304278 | p.Gly450Ser | missense_variant | 0.11 |
Rv1258c | 1406406 | p.Pro312Leu | missense_variant | 0.12 |
embR | 1416457 | c.891G>A | synonymous_variant | 0.12 |
embR | 1417037 | p.Ser104Asn | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472129 | n.284G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472191 | n.346G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474489 | n.832T>G | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1833732 | p.Pro64His | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918367 | p.Ala143Val | missense_variant | 0.12 |
ndh | 2102343 | p.Ala234Thr | missense_variant | 0.12 |
ndh | 2103001 | c.42G>A | synonymous_variant | 0.11 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.25 |
PPE35 | 2168897 | c.1716T>A | synonymous_variant | 0.18 |
PPE35 | 2169600 | p.Asn338Ile | missense_variant | 0.11 |
PPE35 | 2169729 | p.Asn295Ser | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289062 | c.180C>G | synonymous_variant | 0.29 |
pncA | 2290207 | c.-966G>A | upstream_gene_variant | 0.12 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518635 | p.Gly174Asp | missense_variant | 0.13 |
kasA | 2519023 | c.909G>A | synonymous_variant | 0.11 |
folC | 2746677 | p.Ser308Pro | missense_variant | 0.11 |
folC | 2747108 | p.Ala164Val | missense_variant | 0.17 |
pepQ | 2859726 | c.693C>T | synonymous_variant | 0.18 |
Rv2752c | 3066196 | c.-5C>A | upstream_gene_variant | 0.1 |
thyX | 3067321 | c.625C>A | synonymous_variant | 0.29 |
thyA | 3074025 | p.Phe149Leu | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3338993 | c.-125C>T | upstream_gene_variant | 0.11 |
fprA | 3473998 | c.-9G>A | upstream_gene_variant | 1.0 |
fprA | 3473998 | c.-10_-9insA | upstream_gene_variant | 1.0 |
whiB7 | 3568871 | c.-192C>T | upstream_gene_variant | 0.2 |
fbiA | 3641213 | p.Leu224Pro | missense_variant | 0.18 |
fbiB | 3642221 | c.687C>G | synonymous_variant | 0.12 |
clpC1 | 4038507 | p.Leu733Pro | missense_variant | 0.1 |
clpC1 | 4038582 | p.Glu708Val | missense_variant | 0.15 |
panD | 4044307 | c.-26A>G | upstream_gene_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243313 | c.81G>A | synonymous_variant | 0.12 |
embA | 4243829 | c.597C>T | synonymous_variant | 0.33 |
embA | 4244576 | c.1344G>A | synonymous_variant | 0.14 |
embB | 4248216 | p.Arg568His | missense_variant | 0.18 |
embB | 4248393 | p.Ala627Val | missense_variant | 0.13 |
embB | 4248481 | c.1968C>T | synonymous_variant | 0.1 |
ubiA | 4270019 | c.-186A>C | upstream_gene_variant | 0.11 |
ethA | 4327003 | p.Phe157Leu | missense_variant | 0.12 |
ethR | 4327072 | c.-477G>T | upstream_gene_variant | 0.11 |
ethR | 4327864 | p.Gly106Arg | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338712 | c.-191T>C | upstream_gene_variant | 0.1 |