Run ID: SRR22196583
Sample name:
Date: 04-04-2023 04:06:05
Number of reads: 114030
Percentage reads mapped: 96.85
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 |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9099 | p.Leu600Ile | missense_variant | 0.29 |
fgd1 | 491493 | c.711C>A | synonymous_variant | 0.22 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 620319 | c.429C>A | synonymous_variant | 0.33 |
rpoB | 760107 | p.Phe101Val | missense_variant | 0.67 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 764190 | p.Ala274Asp | missense_variant | 0.5 |
rpoC | 764432 | p.Lys355* | stop_gained | 0.4 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801169 | p.Lys121Gln | missense_variant | 0.67 |
embR | 1416373 | c.975C>A | synonymous_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474034 | n.377G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474939 | n.1282C>A | non_coding_transcript_exon_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169850 | p.Asn255Asp | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726499 | p.Leu103Ile | missense_variant | 0.33 |
Rv2752c | 3064820 | p.Gly458Ser | missense_variant | 0.5 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087006 | p.Gln63* | stop_gained | 0.2 |
fbiD | 3339609 | c.492G>T | synonymous_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474496 | p.Arg164Trp | missense_variant | 0.4 |
fprA | 3474774 | c.768G>T | synonymous_variant | 0.5 |
whiB7 | 3568688 | c.-9A>G | upstream_gene_variant | 0.4 |
Rv3236c | 3612534 | p.Ala195Ser | missense_variant | 0.67 |
Rv3236c | 3612655 | c.462G>C | synonymous_variant | 0.5 |
fbiA | 3641332 | p.Gly264Arg | missense_variant | 0.33 |
clpC1 | 4038218 | p.Glu829Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embC | 4242996 | p.Val1045Glu | missense_variant | 0.4 |
embA | 4243725 | p.Glu165* | stop_gained | 0.29 |
embB | 4247476 | c.963C>G | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |