Run ID: SRR6789630
Sample name:
Date: 04-04-2023 16:04:24
Number of reads: 828823
Percentage reads mapped: 92.01
Strain: lineage4.1.1.3
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 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 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 |
fgd1 | 491376 | p.Lys198Asn | missense_variant | 0.11 |
rpoB | 763186 | p.Leu1127Pro | missense_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777892 | p.Gln197* | stop_gained | 0.15 |
mmpS5 | 778514 | p.Val131Glu | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781435 | c.-125G>C | upstream_gene_variant | 1.0 |
fbiC | 1302770 | c.-161T>C | upstream_gene_variant | 0.13 |
fbiC | 1302794 | c.-137A>G | upstream_gene_variant | 0.11 |
fbiC | 1305409 | c.2481delC | frameshift_variant | 0.12 |
Rv1258c | 1406644 | p.Leu233Met | missense_variant | 0.15 |
Rv1258c | 1406943 | c.397_398insGC | frameshift_variant | 0.14 |
Rv1258c | 1406946 | p.Ala132Gly | missense_variant | 0.14 |
Rv1258c | 1406948 | c.391_392delGC | frameshift_variant | 0.14 |
atpE | 1460901 | c.-143delA | upstream_gene_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.14 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.13 |
rpsA | 1834849 | c.1308C>T | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918007 | p.Ala23Asp | missense_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.52 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.52 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288726 | c.516G>A | synonymous_variant | 0.12 |
folC | 2747466 | p.Pro45Ser | missense_variant | 0.13 |
pepQ | 2860154 | p.Glu89Gln | missense_variant | 0.11 |
ribD | 2987290 | p.Asp151Val | missense_variant | 0.11 |
Rv2752c | 3065439 | c.753C>T | synonymous_variant | 0.17 |
thyX | 3067422 | p.Leu175Pro | missense_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339397 | p.Thr94Ser | missense_variant | 0.18 |
fbiD | 3339541 | p.Asp142Asn | missense_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474302 | p.Ala99Asp | missense_variant | 0.17 |
fbiA | 3640439 | c.-104C>T | upstream_gene_variant | 0.12 |
fbiA | 3640450 | c.-93T>C | upstream_gene_variant | 0.11 |
fbiA | 3640546 | p.Lys2Glu | missense_variant | 0.11 |
fbiB | 3642050 | c.516G>T | synonymous_variant | 0.15 |
clpC1 | 4040831 | c.-128delG | upstream_gene_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243396 | p.Ile55Thr | missense_variant | 0.2 |
embA | 4243877 | c.645G>A | synonymous_variant | 0.12 |
embA | 4244007 | p.Ala259Thr | missense_variant | 0.12 |
embA | 4244598 | p.Leu456Met | missense_variant | 0.12 |
embA | 4244625 | p.Leu465Met | missense_variant | 0.13 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.18 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.2 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.2 |
embB | 4247989 | c.1476G>C | synonymous_variant | 0.1 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
ubiA | 4269277 | p.Phe186Ser | missense_variant | 0.12 |
ethR | 4327633 | p.Ile29Phe | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407626 | p.Ala193Thr | missense_variant | 0.11 |
gid | 4407798 | c.405G>T | synonymous_variant | 1.0 |