Run ID: SRR4035747
Sample name:
Date: 04-04-2023 07:16:23
Number of reads: 1349111
Percentage reads mapped: 99.51
Strain: lineage4.1.2
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5136 | c.-104A>G | upstream_gene_variant | 0.11 |
gyrB | 6697 | p.Ile486Met | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7464 | p.Val55Met | missense_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7604 | p.Gln101His | missense_variant | 0.11 |
gyrA | 7698 | p.Arg133Trp | missense_variant | 0.22 |
gyrA | 7705 | p.Thr135Ser | missense_variant | 0.22 |
gyrA | 7855 | p.Met185Lys | missense_variant | 0.13 |
gyrA | 7920 | p.Asn207Asp | missense_variant | 0.14 |
gyrA | 8061 | p.Arg254Cys | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491117 | p.Asn112Ser | missense_variant | 0.12 |
fgd1 | 491135 | p.Tyr118Cys | missense_variant | 0.11 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 576576 | p.Ala410Val | missense_variant | 0.2 |
ccsA | 620165 | p.Leu92Pro | missense_variant | 0.18 |
ccsA | 620330 | p.Ile147Thr | missense_variant | 0.11 |
ccsA | 620665 | p.Trp259Arg | missense_variant | 0.11 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 762703 | p.Val966Glu | missense_variant | 0.13 |
rpoB | 762926 | c.3123delG | frameshift_variant | 0.11 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 764528 | p.Arg387Ser | missense_variant | 0.14 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.95 |
rpoC | 766600 | c.3231C>T | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775912 | p.Arg857Gly | missense_variant | 0.13 |
mmpL5 | 775913 | c.2568C>T | synonymous_variant | 0.14 |
mmpL5 | 775922 | c.2559G>T | synonymous_variant | 0.17 |
mmpL5 | 775946 | c.2535C>T | synonymous_variant | 0.13 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
mmpL5 | 777329 | c.1152C>A | synonymous_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1461108 | p.Ile22Val | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471706 | n.-140A>G | upstream_gene_variant | 0.11 |
rrs | 1472327 | n.482G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472649 | n.804T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472879 | n.1034T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473467 | n.-191A>G | upstream_gene_variant | 0.12 |
rrl | 1475750 | n.2096delC | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475879 | n.2222T>A | non_coding_transcript_exon_variant | 0.4 |
inhA | 1673841 | c.-361A>G | upstream_gene_variant | 0.11 |
inhA | 1674984 | p.Asp261Glu | missense_variant | 0.17 |
rpsA | 1833713 | p.Lys58Glu | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102829 | p.Thr72Ala | missense_variant | 0.1 |
katG | 2156226 | c.-115T>A | upstream_gene_variant | 0.15 |
PPE35 | 2169180 | p.Pro478Leu | missense_variant | 0.14 |
PPE35 | 2169662 | c.951T>C | synonymous_variant | 0.18 |
Rv1979c | 2222533 | p.Ala211Gly | missense_variant | 0.12 |
Rv1979c | 2222822 | p.Ser115Pro | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2519314 | c.1201delT | frameshift_variant | 0.13 |
Rv2752c | 3064691 | p.Pro501Ser | missense_variant | 0.2 |
Rv2752c | 3065287 | p.Leu302Ser | missense_variant | 0.13 |
Rv2752c | 3065728 | p.Ala155Val | missense_variant | 0.18 |
thyA | 3074076 | c.396C>T | synonymous_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3338970 | c.-147delA | upstream_gene_variant | 0.11 |
Rv3083 | 3449497 | p.Lys332Glu | missense_variant | 0.16 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
alr | 3841496 | c.-76A>T | upstream_gene_variant | 0.13 |
clpC1 | 4038753 | p.Gln651Arg | missense_variant | 0.11 |
clpC1 | 4038761 | c.1944C>G | synonymous_variant | 0.11 |
clpC1 | 4039659 | p.Glu349Gly | missense_variant | 0.12 |
clpC1 | 4040526 | p.Arg60His | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244799 | p.Val523Met | missense_variant | 0.18 |
embA | 4244804 | p.Leu524Phe | missense_variant | 0.2 |
embA | 4245066 | p.Phe612Leu | missense_variant | 0.1 |
aftB | 4268002 | c.835C>T | synonymous_variant | 0.12 |
ethR | 4327675 | p.Ala43Thr | missense_variant | 0.13 |
whiB6 | 4338187 | p.Ser112Cys | missense_variant | 0.1 |
whiB6 | 4338414 | p.Gln36His | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |