Run ID: SRR8600107
Sample name:
Date: 04-04-2023 21:34:05
Number of reads: 627225
Percentage reads mapped: 96.13
Strain: La1.8.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.8 | M.bovis | None | None | 1.0 |
La1.8.1 | M.bovis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrB | 6210 | p.Leu324Pro | missense_variant | 0.11 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8094 | p.Gly265Cys | missense_variant | 0.12 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 8741 | c.1440C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9217 | p.Asp639Ala | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576751 | p.Lys468Asn | missense_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 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800970 | p.Tyr54* | stop_gained | 0.12 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1303087 | p.Asp53Tyr | missense_variant | 0.15 |
fbiC | 1304542 | p.Asp538Tyr | missense_variant | 0.15 |
fbiC | 1304833 | p.Pro635Thr | missense_variant | 0.17 |
Rv1258c | 1406751 | p.Gly197Asp | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474265 | n.608G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474269 | n.612C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474287 | n.631_649delCCTTTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474752 | n.1095T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474799 | n.1143delT | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474803 | n.1146_1147insA | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474806 | n.1149A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475427 | n.1770C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476041 | n.2384A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476322 | n.2665C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476707 | n.3050C>A | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.18 |
rpsA | 1834772 | p.Arg411Ser | missense_variant | 0.15 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102193 | p.Arg284Trp | missense_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.15 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.18 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289401 | c.-161delT | upstream_gene_variant | 0.14 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.2 |
ribD | 2986789 | c.-50A>T | upstream_gene_variant | 0.11 |
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 | 3448684 | p.Thr61Ser | missense_variant | 0.15 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
Rv3083 | 3449478 | c.975C>T | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3474445 | p.Gly147Cys | missense_variant | 0.13 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiA | 3641497 | p.Met319Val | missense_variant | 0.1 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4040499 | p.Gln69Arg | missense_variant | 0.11 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241232 | p.Arg457Gln | missense_variant | 0.15 |
embC | 4241689 | c.1827G>A | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242680 | p.Ala940Ser | missense_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248445 | c.1932C>T | synonymous_variant | 0.12 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4268880 | c.-44C>T | upstream_gene_variant | 0.12 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |