Run ID: SRR21677880
Sample name:
Date: 04-04-2023 02:49:13
Number of reads: 109420
Percentage reads mapped: 99.15
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7089 | p.Asp617Val | missense_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7742 | c.441G>A | synonymous_variant | 0.33 |
gyrA | 8015 | p.Gln238His | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 620499 | c.609G>A | synonymous_variant | 0.29 |
rpoB | 759881 | c.75C>A | synonymous_variant | 0.25 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.5 |
rpoC | 763333 | c.-37G>A | upstream_gene_variant | 0.25 |
rpoC | 763365 | c.-4delT | upstream_gene_variant | 0.33 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775921 | p.Leu854Met | missense_variant | 0.5 |
fbiC | 1304851 | p.Gly641Cys | missense_variant | 0.4 |
Rv1258c | 1406745 | p.Pro199Leu | missense_variant | 0.67 |
Rv1258c | 1406936 | c.405A>G | synonymous_variant | 0.4 |
embR | 1417112 | p.Leu79Pro | missense_variant | 0.29 |
atpE | 1461236 | c.192C>T | synonymous_variant | 0.5 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472583 | n.738T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474207 | n.550C>A | non_coding_transcript_exon_variant | 0.33 |
fabG1 | 1673462 | p.Gly8Val | missense_variant | 0.67 |
inhA | 1674924 | c.723G>C | synonymous_variant | 0.5 |
rpsA | 1833478 | c.-64G>A | upstream_gene_variant | 1.0 |
rpsA | 1834302 | p.Val254Asp | missense_variant | 0.25 |
katG | 2154868 | p.Leu415Pro | missense_variant | 0.25 |
katG | 2156127 | c.-16T>C | upstream_gene_variant | 0.5 |
PPE35 | 2169382 | p.Trp411Arg | missense_variant | 0.25 |
PPE35 | 2169758 | c.855C>A | synonymous_variant | 0.18 |
Rv1979c | 2221758 | c.1407A>T | synonymous_variant | 0.29 |
Rv1979c | 2222549 | p.Ser206Pro | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518151 | p.Ser13Gly | missense_variant | 0.5 |
eis | 2714199 | p.Lys378Asn | missense_variant | 0.4 |
ribD | 2987006 | c.170delG | frameshift_variant | 0.29 |
ribD | 2987542 | p.Leu235Arg | missense_variant | 0.25 |
Rv2752c | 3065425 | p.Gly256Val | missense_variant | 0.22 |
thyX | 3067487 | p.Lys153Asn | missense_variant | 0.67 |
thyA | 3073692 | c.780A>G | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449215 | p.Trp238Arg | missense_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474576 | c.570T>C | synonymous_variant | 0.25 |
fprA | 3475055 | p.Gly350Asp | missense_variant | 0.22 |
fbiB | 3642532 | p.Arg333Leu | missense_variant | 0.22 |
rpoA | 3878327 | p.His61Asp | missense_variant | 0.4 |
ddn | 3986779 | c.-65A>G | upstream_gene_variant | 0.18 |
ddn | 3986857 | p.Pro5Gln | missense_variant | 0.18 |
ddn | 3986874 | p.Ser11Pro | missense_variant | 0.18 |
embC | 4240871 | p.Val337Ile | missense_variant | 0.4 |
embC | 4241233 | c.1371G>T | synonymous_variant | 0.29 |
embC | 4241846 | p.Thr662Ala | missense_variant | 0.67 |
embC | 4242085 | c.2223A>C | synonymous_variant | 0.33 |
embC | 4242489 | p.Gln876Pro | missense_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4248381 | p.Arg623Pro | missense_variant | 0.25 |
aftB | 4267665 | p.Asn391Ser | missense_variant | 0.67 |
aftB | 4267768 | p.Leu357Met | missense_variant | 0.18 |
aftB | 4267858 | c.978dupG | frameshift_variant | 0.4 |
ubiA | 4269161 | p.Ser225Pro | missense_variant | 0.29 |
ethA | 4326457 | p.Ile339Met | missense_variant | 0.29 |
ethA | 4327262 | p.Gly71Val | missense_variant | 0.5 |
ethA | 4327782 | c.-309C>G | upstream_gene_variant | 0.18 |