Run ID: SRR6045859
Sample name:
Date: 04-04-2023 12:06:50
Number of reads: 2979446
Percentage reads mapped: 96.53
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gid | 4408087 | c.115delC | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.99 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.99 |
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 |
embR | 1416561 | p.Lys263Glu | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472543 | n.699_700delCA | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472891 | n.1046A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474292 | n.635T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475686 | n.2029C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.19 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474460 | p.Val152Ile | missense_variant | 1.0 |
fbiA | 3641453 | p.Arg304Gln | missense_variant | 1.0 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
rpoA | 3878567 | c.-60C>G | upstream_gene_variant | 0.29 |
embC | 4241465 | p.Phe535Ile | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |