Run ID: SRR4037758
Sample name:
Date: 04-04-2023 07:38:28
Number of reads: 344917
Percentage reads mapped: 99.68
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5678 | p.Ser147Ala | missense_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7874 | c.573G>A | synonymous_variant | 0.25 |
gyrA | 9138 | p.Gln613Glu | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491706 | c.924G>T | synonymous_variant | 0.33 |
ccsA | 619741 | c.-150G>A | upstream_gene_variant | 0.67 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.4 |
rpoB | 759855 | p.Arg17Ser | missense_variant | 0.22 |
rpoB | 762663 | p.Leu953Met | missense_variant | 0.29 |
rpoC | 763584 | p.Gly72Asp | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.19 |
mmpL5 | 776232 | p.Pro750Gln | missense_variant | 0.17 |
mmpL5 | 776850 | p.Gln544Arg | missense_variant | 0.29 |
mmpL5 | 776964 | p.Thr506Ile | missense_variant | 0.15 |
mmpL5 | 777416 | c.1065G>T | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303151 | p.Gly74Asp | missense_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475268 | n.1613_1615delGAG | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476730 | n.3073G>T | non_coding_transcript_exon_variant | 0.15 |
inhA | 1673363 | c.-839G>A | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168479 | p.Thr712Pro | missense_variant | 1.0 |
PPE35 | 2168516 | c.2097C>A | synonymous_variant | 0.5 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.5 |
PPE35 | 2169595 | p.Gly340Cys | missense_variant | 0.18 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289367 | c.-127delG | upstream_gene_variant | 0.25 |
folC | 2746660 | c.938delT | frameshift_variant | 0.67 |
folC | 2747296 | c.303G>A | synonymous_variant | 0.29 |
pepQ | 2860313 | p.Phe36Leu | missense_variant | 0.29 |
Rv2752c | 3066175 | p.Pro6Arg | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568779 | c.-100T>C | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 0.75 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.4 |
fbiB | 3642547 | p.Gly338Val | missense_variant | 0.4 |
clpC1 | 4039314 | p.Arg464His | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |