Run ID: SRR4035578
Sample name:
Date: 04-04-2023 07:11:26
Number of reads: 1212842
Percentage reads mapped: 99.68
Strain: lineage4.3.4.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.95 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777174 | p.Arg436His | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801048 | p.Tyr80* | stop_gained | 0.13 |
embR | 1417179 | c.167_168dupTC | frameshift_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475025 | n.1368A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475132 | n.1475T>C | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.16 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.17 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.18 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.18 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.19 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.13 |
rpsA | 1833470 | c.-72T>C | upstream_gene_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102939 | p.Arg35Gln | missense_variant | 0.12 |
katG | 2153933 | p.Ala727Ser | missense_variant | 0.38 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.36 |
Rv1979c | 2222185 | c.979delT | frameshift_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726526 | p.Ser112Thr | missense_variant | 0.18 |
Rv2752c | 3065817 | c.375C>T | synonymous_variant | 0.17 |
thyX | 3067343 | c.603C>T | synonymous_variant | 0.2 |
thyX | 3067896 | p.Phe17Ser | missense_variant | 0.12 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449950 | c.1447C>T | synonymous_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568476 | c.204T>C | synonymous_variant | 0.15 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.67 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4242203 | p.Leu781Met | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246642 | c.129G>A | synonymous_variant | 0.17 |
embB | 4247068 | c.555T>C | synonymous_variant | 0.22 |
embB | 4247441 | p.Ala310Thr | missense_variant | 0.14 |
aftB | 4267191 | p.Gly549Asp | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |