Run ID: SRR1172267
Sample name:
Date: 03-04-2023 03:01:53
Number of reads: 2453880
Percentage reads mapped: 88.0
Strain: lineage1.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9047 | c.1746C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9443 | c.2142G>A | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576000 | p.Asp218Ala | missense_variant | 1.0 |
rpoB | 760490 | c.684C>T | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 766252 | c.2883G>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776395 | p.Phe696Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472814 | n.969G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473038 | n.1193A>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473070 | n.1225G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473071 | n.1226C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473094 | n.1249T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476483 | n.2826G>A | non_coding_transcript_exon_variant | 0.15 |
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 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2168234 | c.2379G>A | synonymous_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.19 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ribD | 2987540 | c.702G>A | synonymous_variant | 1.0 |
Rv2752c | 3064557 | p.Tyr545* | stop_gained | 1.0 |
Rv2752c | 3065527 | p.Leu222Pro | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
ddn | 3987057 | p.Arg72Trp | missense_variant | 1.0 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_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 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
Rv2752c | 3064553 | c.664_1638del | conservative_inframe_deletion | 1.0 |