Run ID: SRR6789618
Sample name:
Date: 04-04-2023 16:03:45
Number of reads: 723714
Percentage reads mapped: 98.89
Strain: lineage4.9.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
lineage4.9.1 | Euro-American (H37Rv-like) | T1 | 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 | 8978 | c.1677C>T | synonymous_variant | 1.0 |
mshA | 576307 | c.960C>T | synonymous_variant | 0.14 |
mshA | 576527 | p.Glu394* | stop_gained | 0.14 |
ccsA | 619848 | c.-43C>T | upstream_gene_variant | 0.11 |
ccsA | 620176 | p.Val96Leu | missense_variant | 0.12 |
rpoB | 760133 | c.327C>G | synonymous_variant | 0.18 |
rpoB | 763196 | p.Glu1130Asp | missense_variant | 0.13 |
rpoB | 763231 | p.Arg1142His | missense_variant | 0.12 |
rpoC | 765558 | p.Thr730Met | missense_variant | 0.1 |
rpoC | 766038 | p.Asp890Val | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407142 | p.Asp67Asn | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.16 |
fabG1 | 1673756 | p.Glu106Gly | missense_variant | 0.13 |
rpsA | 1834816 | p.His425Gln | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918062 | p.Lys41Asn | missense_variant | 0.1 |
ndh | 2101744 | p.Asp433Glu | missense_variant | 0.12 |
PPE35 | 2169041 | c.1572G>A | synonymous_variant | 0.67 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 0.33 |
PPE35 | 2169047 | p.Ile522Val | missense_variant | 0.2 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
PPE35 | 2169056 | c.1557A>G | synonymous_variant | 0.2 |
PPE35 | 2169059 | c.1554G>A | synonymous_variant | 0.8 |
PPE35 | 2169063 | p.Met517Thr | missense_variant | 1.0 |
PPE35 | 2169065 | p.Ala516Ile | missense_variant | 0.8 |
PPE35 | 2169068 | c.1545G>T | synonymous_variant | 0.8 |
PPE35 | 2169071 | c.1542A>G | synonymous_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.35 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.34 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289138 | p.Leu35Arg | missense_variant | 1.0 |
pncA | 2289468 | c.-227G>C | upstream_gene_variant | 0.14 |
kasA | 2518041 | c.-74T>A | upstream_gene_variant | 0.11 |
kasA | 2518721 | c.608delA | frameshift_variant | 0.12 |
ribD | 2987140 | p.Val101Asp | missense_variant | 0.14 |
Rv2752c | 3064798 | p.Arg465Leu | missense_variant | 0.13 |
thyX | 3067408 | p.Glu180Gln | missense_variant | 0.17 |
thyX | 3067703 | p.Tyr81* | stop_gained | 0.12 |
fbiD | 3339385 | p.Asp90Asn | missense_variant | 1.0 |
whiB7 | 3568525 | p.Cys52Phe | missense_variant | 0.12 |
whiB7 | 3568645 | p.Arg12Lys | missense_variant | 0.13 |
Rv3236c | 3612157 | p.Arg320Gln | missense_variant | 0.12 |
fbiA | 3640381 | c.-162T>C | upstream_gene_variant | 0.11 |
fbiB | 3642395 | c.861A>T | synonymous_variant | 0.12 |
embA | 4244262 | p.Leu344Met | missense_variant | 0.15 |
embA | 4245886 | p.Asp885Val | missense_variant | 0.12 |
ethA | 4326063 | p.Gly471Cys | missense_variant | 0.15 |
ethA | 4326067 | c.1407G>T | synonymous_variant | 0.15 |
ethA | 4326109 | p.Trp455Cys | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |