Run ID: ERR4132443
Sample name:
Date: 01-04-2023 04:30:16
Number of reads: 470661
Percentage reads mapped: 99.03
Strain: lineage4.1
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9426 | p.Asp709Asn | missense_variant | 0.11 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.36 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 764263 | c.894G>A | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765630 | p.Asp754Val | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776002 | p.Leu827Met | missense_variant | 0.22 |
mmpL5 | 776028 | p.Leu818Arg | missense_variant | 0.22 |
mmpL5 | 777320 | c.1161C>G | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303574 | p.Leu215Pro | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673945 | p.Arg169Leu | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.36 |
katG | 2154057 | c.2055C>T | synonymous_variant | 0.12 |
PPE35 | 2168371 | p.Ala748Thr | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.5 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.4 |
ahpC | 2726350 | p.Trp53Leu | missense_variant | 0.22 |
folC | 2746885 | c.714C>A | synonymous_variant | 0.15 |
ribD | 2987102 | c.264G>T | synonymous_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448407 | c.-97A>G | upstream_gene_variant | 0.25 |
Rv3083 | 3448410 | c.-94A>T | upstream_gene_variant | 0.25 |
Rv3083 | 3449756 | p.Tyr418Phe | missense_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474998 | p.Gly331Asp | missense_variant | 0.15 |
whiB7 | 3568757 | c.-78A>T | upstream_gene_variant | 0.25 |
whiB7 | 3568849 | c.-170C>T | upstream_gene_variant | 0.2 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 1.0 |
fbiA | 3640765 | p.Pro75Thr | missense_variant | 0.14 |
fbiB | 3642748 | p.Ala405Asp | missense_variant | 0.22 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.2 |
panD | 4044270 | c.12G>A | synonymous_variant | 0.14 |
panD | 4044337 | c.-56G>T | upstream_gene_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4245437 | p.Met735Ile | missense_variant | 0.25 |
embB | 4247068 | c.555T>C | synonymous_variant | 0.4 |
embB | 4249155 | p.Gly881Val | missense_variant | 0.33 |
aftB | 4267130 | c.1707C>G | synonymous_variant | 0.14 |
aftB | 4268158 | p.Phe227Val | missense_variant | 1.0 |
ethA | 4327968 | c.-495C>A | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |