Run ID: SRR833158
Sample name:
Date: 04-04-2023 21:11:50
Number of reads: 199808
Percentage reads mapped: 76.63
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6100 | c.861G>T | synonymous_variant | 0.22 |
gyrB | 6128 | p.Tyr297His | missense_variant | 0.2 |
gyrA | 6865 | c.-437G>T | upstream_gene_variant | 0.22 |
gyrB | 7008 | p.Leu590Arg | missense_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491187 | c.405G>A | synonymous_variant | 0.67 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760791 | p.Glu329Lys | missense_variant | 0.29 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.75 |
rpoB | 763235 | p.Glu1143Asp | missense_variant | 0.22 |
rpoC | 763487 | p.Lys40Glu | missense_variant | 0.25 |
mmpL5 | 775719 | p.Val921Gly | missense_variant | 0.29 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801380 | p.Val191Ala | missense_variant | 0.25 |
fbiC | 1302772 | c.-159T>G | upstream_gene_variant | 0.67 |
fbiC | 1303234 | p.Cys102Arg | missense_variant | 0.2 |
fbiC | 1305353 | p.Gly808Ala | missense_variant | 1.0 |
Rv1258c | 1406714 | c.627A>G | synonymous_variant | 0.67 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475343 | n.1686A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475344 | n.1687G>A | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673270 | c.-170G>C | upstream_gene_variant | 0.33 |
rpsA | 1833536 | c.-6A>G | upstream_gene_variant | 0.22 |
rpsA | 1833540 | c.-2A>C | upstream_gene_variant | 0.22 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
ndh | 2101929 | p.Thr372Ala | missense_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167911 | p.Ala901Gly | missense_variant | 1.0 |
PPE35 | 2167915 | p.Asn900Asp | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168683 | c.1927_1929delACC | conservative_inframe_deletion | 0.25 |
Rv1979c | 2223133 | p.Ile11Ser | missense_variant | 0.33 |
eis | 2715071 | p.Ala88Pro | missense_variant | 1.0 |
eis | 2715441 | c.-109C>T | upstream_gene_variant | 1.0 |
ahpC | 2726533 | c.347_362delGCGAACTCAGCCAAGC | frameshift_variant | 0.33 |
ahpC | 2726635 | p.Ser148Leu | missense_variant | 1.0 |
pepQ | 2860385 | p.Ala12Thr | missense_variant | 0.29 |
Rv2752c | 3065931 | c.261C>T | synonymous_variant | 0.4 |
thyA | 3073902 | p.Ala190Gly | missense_variant | 0.4 |
thyA | 3073906 | p.Ala189Gly | missense_variant | 0.4 |
thyA | 3074130 | c.342G>T | synonymous_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087147 | p.Ser110Pro | missense_variant | 0.5 |
ald | 3087818 | p.Cys333* | stop_gained | 1.0 |
Rv3083 | 3448423 | c.-81C>A | upstream_gene_variant | 0.25 |
Rv3083 | 3448425 | c.-79_-78delATinsGC | upstream_gene_variant | 0.25 |
Rv3083 | 3448427 | c.-77C>G | upstream_gene_variant | 0.25 |
Rv3083 | 3449892 | c.1389C>T | synonymous_variant | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568768 | c.-89A>G | upstream_gene_variant | 0.29 |
whiB7 | 3568773 | c.-95_-94insCTGC | upstream_gene_variant | 0.29 |
whiB7 | 3568867 | c.-188A>G | upstream_gene_variant | 0.33 |
whiB7 | 3568869 | c.-190C>G | upstream_gene_variant | 0.33 |
rpoA | 3878194 | p.Val105Gly | missense_variant | 0.67 |
ddn | 3986997 | p.Thr52Ser | missense_variant | 0.67 |
clpC1 | 4038540 | p.Leu722Gln | missense_variant | 0.17 |
clpC1 | 4040634 | p.Asn24Ile | missense_variant | 0.13 |
embA | 4244725 | p.Asp498Ala | missense_variant | 0.33 |
embA | 4246112 | c.2881_2884delGTTC | frameshift_variant | 0.33 |
embA | 4246120 | p.Val963Ala | missense_variant | 0.33 |
embB | 4246421 | c.-93G>A | upstream_gene_variant | 1.0 |
embB | 4247474 | p.Arg321Ser | missense_variant | 0.33 |
embB | 4247476 | c.964delT | frameshift_variant | 0.33 |
aftB | 4267124 | c.1713T>A | synonymous_variant | 0.5 |
ubiA | 4269188 | p.Thr216Pro | missense_variant | 0.5 |
ubiA | 4269190 | p.Ser215Thr | missense_variant | 0.5 |
ubiA | 4269482 | p.Trp118Arg | missense_variant | 0.25 |
ethA | 4327199 | p.Tyr92Ser | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408466 | c.-264C>T | upstream_gene_variant | 0.5 |