Run ID: SRR17156538
Sample name:
Date: 03-04-2023 17:54:52
Number of reads: 338068
Percentage reads mapped: 99.51
Strain: La2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La2 | M.caprae | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 6922 | c.-380G>T | upstream_gene_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7871 | c.570G>T | synonymous_variant | 0.15 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576178 | c.831G>A | synonymous_variant | 0.2 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776159 | c.2322T>C | synonymous_variant | 0.14 |
mmpL5 | 776839 | p.Asp548Asn | missense_variant | 1.0 |
mmpL5 | 778051 | p.Gly144Ser | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1305248 | p.Ala773Val | missense_variant | 0.12 |
Rv1258c | 1406873 | c.468C>G | synonymous_variant | 0.17 |
Rv1258c | 1407255 | p.Ala29Val | missense_variant | 1.0 |
embR | 1417042 | c.306G>T | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473043 | n.1198G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473284 | n.1439A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474153 | n.496C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474355 | n.698A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474675 | n.1018C>A | non_coding_transcript_exon_variant | 0.33 |
inhA | 1673766 | c.-436C>T | upstream_gene_variant | 1.0 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102194 | p.Ser283Arg | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155291 | p.Lys274Thr | missense_variant | 0.12 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2167681 | p.Ser978Pro | missense_variant | 0.14 |
PPE35 | 2167907 | c.2706A>G | synonymous_variant | 0.22 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170149 | p.His155Arg | missense_variant | 0.17 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715035 | p.Met100Val | missense_variant | 1.0 |
ribD | 2987239 | p.Thr134Asn | missense_variant | 0.18 |
Rv2752c | 3065118 | c.1074C>T | synonymous_variant | 1.0 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
Rv3083 | 3448330 | c.-174A>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
clpC1 | 4038353 | c.2352G>A | synonymous_variant | 0.25 |
clpC1 | 4039569 | p.Met379Thr | missense_variant | 0.12 |
clpC1 | 4040241 | p.Thr155Ile | missense_variant | 0.11 |
clpC1 | 4040250 | p.Glu152Gly | missense_variant | 0.11 |
embC | 4240508 | p.Ala216Thr | missense_variant | 0.13 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4243190 | c.-43G>A | upstream_gene_variant | 1.0 |
embA | 4243779 | p.Pro183Thr | missense_variant | 0.11 |
embA | 4244117 | c.885G>T | synonymous_variant | 0.12 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247602 | c.1089G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4268008 | p.Gly277Arg | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269523 | p.Thr104Ile | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4327277 | p.Phe66Tyr | missense_variant | 0.12 |
ethA | 4327362 | p.Arg38Trp | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |