Run ID: ERR4817448
Sample name:
Date: 01-04-2023 14:59:56
Number of reads: 420003
Percentage reads mapped: 99.36
Strain: lineage6.3.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage6 | West-Africa 2 | AFRI_1 | RD702 | 1.0 |
lineage6.3 | West-Africa 2 | AFRI_1 | RD702 | 1.0 |
lineage6.3.1 | West-Africa 2 | AFRI_1 | RD702 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrB | 6464 | p.Lys409Gln | missense_variant | 0.14 |
gyrA | 7322 | c.21G>T | synonymous_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7629 | p.Val110Met | missense_variant | 0.22 |
gyrA | 8530 | p.Ala410Val | missense_variant | 0.25 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9789 | p.Ala830Ser | missense_variant | 0.29 |
fgd1 | 491668 | p.Lys296Glu | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760969 | p.Ser388Leu | missense_variant | 1.0 |
rpoB | 761548 | p.Val581Ala | missense_variant | 0.12 |
rpoB | 761674 | p.Gly623Val | missense_variant | 0.2 |
rpoB | 761723 | p.Glu639Asp | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764444 | p.Asp359Tyr | missense_variant | 0.14 |
rpoC | 764953 | c.1584G>T | synonymous_variant | 0.12 |
rpoC | 766599 | p.Tyr1077Ser | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776305 | p.Pro726Ser | missense_variant | 0.29 |
mmpL5 | 776546 | p.Met645Ile | missense_variant | 0.2 |
mmpR5 | 778154 | c.-836G>A | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800780 | c.-29C>T | upstream_gene_variant | 0.15 |
rplC | 801453 | c.645T>C | synonymous_variant | 0.22 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1303018 | c.88C>T | synonymous_variant | 0.14 |
embR | 1417023 | p.Thr109Ser | missense_variant | 0.4 |
atpE | 1461251 | c.207G>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472608 | n.767delG | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473174 | n.1329G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474421 | n.764G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474549 | n.892G>T | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673392 | c.-48G>C | upstream_gene_variant | 0.18 |
inhA | 1674434 | p.Val78Ala | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102694 | p.Val117Ile | missense_variant | 1.0 |
katG | 2154128 | p.Leu662Phe | missense_variant | 0.13 |
katG | 2154562 | p.Val517Ala | missense_variant | 0.2 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155080 | c.1032G>A | synonymous_variant | 0.25 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156550 | c.-439G>C | upstream_gene_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169593 | c.1020C>T | synonymous_variant | 0.25 |
PPE35 | 2169752 | c.861C>T | synonymous_variant | 0.33 |
Rv1979c | 2221932 | c.1233G>T | synonymous_variant | 0.14 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222852 | p.Ala105Thr | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518077 | c.-38G>A | upstream_gene_variant | 0.4 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518140 | p.Gly9Val | missense_variant | 0.13 |
eis | 2714603 | p.Val244Ile | missense_variant | 0.13 |
ribD | 2987179 | p.Val114Asp | missense_variant | 0.25 |
Rv2752c | 3064671 | c.1521C>T | synonymous_variant | 1.0 |
Rv2752c | 3065024 | p.Pro390Ser | missense_variant | 0.25 |
Rv2752c | 3065905 | p.Leu96Arg | missense_variant | 0.13 |
thyX | 3067939 | p.Glu3* | stop_gained | 0.2 |
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 |
ald | 3087228 | p.Ala137Thr | missense_variant | 0.22 |
ald | 3087725 | c.906C>A | synonymous_variant | 0.12 |
Rv3083 | 3448833 | c.330G>A | synonymous_variant | 0.29 |
Rv3083 | 3449195 | p.Gly231Asp | missense_variant | 0.18 |
Rv3083 | 3449781 | c.1278G>A | synonymous_variant | 1.0 |
fprA | 3473963 | c.-44G>T | upstream_gene_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612969 | p.Gly50Trp | missense_variant | 0.15 |
fbiA | 3640492 | c.-51G>T | upstream_gene_variant | 0.14 |
alr | 3840610 | p.Leu271Met | missense_variant | 0.29 |
rpoA | 3877629 | c.879C>T | synonymous_variant | 0.15 |
rpoA | 3877696 | p.Thr271Ile | missense_variant | 1.0 |
rpoA | 3878052 | c.456C>T | synonymous_variant | 0.33 |
ddn | 3986704 | c.-140C>A | upstream_gene_variant | 0.2 |
ddn | 3986985 | p.Leu48Met | missense_variant | 0.17 |
clpC1 | 4038816 | p.Ala630Glu | missense_variant | 0.13 |
clpC1 | 4039040 | c.1665C>A | synonymous_variant | 0.22 |
clpC1 | 4040166 | p.Ala180Val | missense_variant | 0.18 |
clpC1 | 4040365 | c.340C>A | synonymous_variant | 0.18 |
panD | 4043985 | c.297C>T | synonymous_variant | 0.18 |
embC | 4240002 | p.Thr47Ile | missense_variant | 0.15 |
embC | 4240313 | p.Thr151Ala | missense_variant | 0.17 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241658 | p.Ser599* | stop_gained | 0.18 |
embC | 4241843 | p.Leu661Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242946 | c.-287T>C | upstream_gene_variant | 0.25 |
embA | 4243213 | c.-20G>A | upstream_gene_variant | 0.22 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244379 | p.Pro383Ser | missense_variant | 1.0 |
embA | 4244821 | p.Gly530Ala | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249516 | c.3003G>A | synonymous_variant | 0.13 |
aftB | 4268345 | c.492C>A | synonymous_variant | 0.5 |
aftB | 4268477 | c.360C>T | synonymous_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269522 | c.-686C>T | upstream_gene_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethA | 4326331 | c.1143C>A | synonymous_variant | 0.15 |
ethA | 4326465 | p.Ile337Val | missense_variant | 1.0 |
whiB6 | 4338592 | c.-71G>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408306 | c.-104C>T | upstream_gene_variant | 0.25 |