Run ID: SRR13837514
Sample name:
Date: 03-04-2023 09:12:12
Number of reads: 593220
Percentage reads mapped: 97.92
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5922 | p.Glu228Gly | missense_variant | 1.0 |
gyrB | 7242 | p.Lys668Thr | missense_variant | 1.0 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.13 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.12 |
gyrA | 7571 | c.270G>C | synonymous_variant | 0.18 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.11 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.12 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.12 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.11 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.17 |
gyrA | 7760 | c.459C>T | synonymous_variant | 0.17 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.18 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.16 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.12 |
gyrA | 7838 | c.537C>G | synonymous_variant | 0.11 |
ccsA | 620360 | p.Tyr157Ser | missense_variant | 1.0 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.14 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.11 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.12 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.12 |
rpoB | 760845 | p.Thr347Pro | missense_variant | 0.12 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.12 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.14 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.13 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.13 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.14 |
rpoB | 761356 | c.1550_1551insA | frameshift_variant | 1.0 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.12 |
rpoC | 763347 | c.-23C>G | upstream_gene_variant | 1.0 |
rpoC | 763402 | c.33C>G | synonymous_variant | 0.11 |
rpoC | 763414 | c.45T>C | synonymous_variant | 0.11 |
rpoC | 766025 | p.Val886Met | missense_variant | 1.0 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.11 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.17 |
mmpL5 | 776145 | p.Ala779Gly | missense_variant | 1.0 |
mmpL5 | 776954 | p.Lys509Asn | missense_variant | 1.0 |
rplC | 801231 | c.423C>A | synonymous_variant | 1.0 |
atpE | 1460916 | c.-129G>A | upstream_gene_variant | 1.0 |
rrs | 1472756 | n.911A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476201 | n.2544C>G | non_coding_transcript_exon_variant | 1.0 |
katG | 2155137 | c.975G>C | synonymous_variant | 1.0 |
PPE35 | 2168892 | p.Thr574Lys | missense_variant | 1.0 |
Rv1979c | 2222852 | p.Ala105Thr | missense_variant | 1.0 |
ribD | 2987259 | p.Leu141Val | missense_variant | 1.0 |
Rv2752c | 3065161 | p.Asn344Thr | missense_variant | 1.0 |
Rv2752c | 3065830 | p.Ile121Thr | missense_variant | 0.93 |
Rv2752c | 3067100 | c.-909G>A | upstream_gene_variant | 1.0 |
thyA | 3074076 | c.396C>G | synonymous_variant | 0.12 |
thyA | 3074106 | c.366T>C | synonymous_variant | 0.13 |
thyA | 3074117 | c.355C>T | synonymous_variant | 0.12 |
thyA | 3074120 | c.352T>C | synonymous_variant | 0.12 |
thyA | 3074130 | c.342G>C | synonymous_variant | 0.13 |
thyA | 3074157 | c.315C>G | synonymous_variant | 0.13 |
thyA | 3074160 | c.312A>G | synonymous_variant | 0.13 |
thyA | 3074163 | p.Ala103Thr | missense_variant | 0.13 |
thyA | 3074172 | c.300G>C | synonymous_variant | 0.12 |
thyA | 3074205 | p.Glu89Asp | missense_variant | 0.11 |
fbiD | 3339117 | c.-1C>T | upstream_gene_variant | 1.0 |
Rv3083 | 3448661 | p.Val53Ala | missense_variant | 1.0 |
Rv3236c | 3612041 | p.Val359Glu | missense_variant | 1.0 |
fbiA | 3640418 | c.-125C>A | upstream_gene_variant | 1.0 |
rpoA | 3877877 | p.Ala211Ser | missense_variant | 1.0 |
ddn | 3986699 | c.-145C>G | upstream_gene_variant | 0.12 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.11 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.12 |
clpC1 | 4039250 | c.1455C>G | synonymous_variant | 0.92 |
embC | 4242113 | c.2251C>T | synonymous_variant | 1.0 |
embB | 4246367 | c.-147C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338567 | c.-46C>T | upstream_gene_variant | 0.96 |
gid | 4408302 | c.-101delC | upstream_gene_variant | 1.0 |