Run ID: SRR1175108
Sample name:
Date: 03-04-2023 03:37:52
Number of reads: 1759054
Percentage reads mapped: 93.39
Strain: lineage3.1.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.2 | East-African-Indian | CAS;CAS2 | RD750 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gid | 4407967 | p.Leu79Ser | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5786 | p.Thr183Ala | missense_variant | 1.0 |
gyrB | 5981 | p.Ser248Gly | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
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 | 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 |
Rv1258c | 1406242 | p.Ala367Thr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918104 | c.165G>A | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156400 | c.-289G>A | upstream_gene_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168604 | p.Pro670Leu | missense_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.29 |
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 | 0.97 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339153 | p.Leu12Phe | missense_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_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 |