Run ID: ERR4813243
Sample name:
Date: 01-04-2023 12:37:30
Number of reads: 795208
Percentage reads mapped: 99.65
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5309 | p.Glu24Lys | missense_variant | 0.12 |
gyrB | 5314 | c.75C>G | synonymous_variant | 0.12 |
gyrB | 5862 | p.Leu208Gln | missense_variant | 0.12 |
gyrB | 6627 | p.Ala463Gly | missense_variant | 0.12 |
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 | 491102 | p.Thr107Ile | missense_variant | 0.11 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.24 |
rpoB | 759653 | c.-154C>A | upstream_gene_variant | 0.17 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760282 | p.Thr159Lys | missense_variant | 0.2 |
rpoB | 762684 | p.Ala960Pro | missense_variant | 0.11 |
rpoB | 763096 | p.Tyr1097Cys | missense_variant | 0.11 |
rpoB | 763109 | c.3305delA | frameshift_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 767070 | p.Thr1234Ser | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776335 | p.Val716Met | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472699 | n.854G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474286 | n.629C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474672 | n.1015C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475807 | n.2150A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475904 | n.2247G>A | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1673267 | c.-173C>T | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102543 | p.Arg167Leu | missense_variant | 0.12 |
ndh | 2102846 | p.Gly66Val | missense_variant | 0.18 |
katG | 2156199 | c.-88G>A | upstream_gene_variant | 0.14 |
katG | 2156370 | c.-259T>G | upstream_gene_variant | 1.0 |
PPE35 | 2167931 | c.2682C>A | synonymous_variant | 0.13 |
PPE35 | 2169529 | p.Leu362Val | missense_variant | 0.25 |
PPE35 | 2169894 | p.Gly240Asp | missense_variant | 0.17 |
Rv1979c | 2222169 | c.996C>T | synonymous_variant | 0.12 |
Rv1979c | 2222794 | p.Asp124Gly | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2715089 | p.Leu82Ile | missense_variant | 0.14 |
Rv2752c | 3064876 | p.Ser439Tyr | missense_variant | 0.12 |
thyX | 3067388 | c.558C>A | synonymous_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449127 | c.624G>T | synonymous_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640510 | c.-33G>T | upstream_gene_variant | 0.15 |
clpC1 | 4038588 | p.Arg706His | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244708 | c.1476C>T | synonymous_variant | 0.15 |
ethA | 4326232 | c.1242T>C | synonymous_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |