Run ID: SRR6855768
Sample name:
Date: 04-04-2023 17:44:58
Number of reads: 381184
Percentage reads mapped: 89.46
Strain: lineage4.3.2.1
Drug-resistance: Other
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 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 0.99 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1918388 | c.451delG | frameshift_variant | 0.18 | capreomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 0.94 |
gyrB | 5687 | p.Tyr150His | missense_variant | 0.1 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8374 | c.1075delG | frameshift_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490618 | c.-165T>C | upstream_gene_variant | 0.11 |
fgd1 | 491168 | p.Phe129Ser | missense_variant | 0.1 |
fgd1 | 491584 | c.803delT | frameshift_variant | 0.11 |
mshA | 575690 | p.Gly115Arg | missense_variant | 0.12 |
rpoB | 762183 | c.2380delG | frameshift_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 766192 | c.2824delC | frameshift_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776372 | c.2109C>G | synonymous_variant | 0.12 |
mmpL5 | 776515 | p.His656Asp | missense_variant | 0.18 |
mmpL5 | 777258 | c.1222dupC | frameshift_variant | 0.1 |
mmpL5 | 777721 | p.Arg254Trp | missense_variant | 0.12 |
mmpL5 | 778912 | c.-432G>T | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781515 | c.-45G>A | upstream_gene_variant | 0.12 |
rplC | 800843 | p.Gly12Asp | missense_variant | 0.12 |
fbiC | 1303034 | p.Asp35Val | missense_variant | 0.14 |
Rv1258c | 1406802 | c.538delG | frameshift_variant | 0.14 |
Rv1258c | 1407157 | p.Ala62Thr | missense_variant | 0.12 |
embR | 1416258 | p.Asn364Asp | missense_variant | 0.11 |
atpE | 1461092 | c.49delA | frameshift_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472518 | n.673G>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472678 | n.833T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472679 | n.834T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472682 | n.839_843delGGGAT | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472701 | n.856T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475404 | n.1747A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673526 | c.87_88insT | frameshift_variant | 0.2 |
inhA | 1673535 | c.-667A>C | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102645 | c.395_397dupCCG | conservative_inframe_insertion | 0.29 |
PPE35 | 2169075 | p.Ile513Thr | missense_variant | 0.12 |
Rv1979c | 2222493 | c.672C>T | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746523 | c.1075delG | frameshift_variant | 0.14 |
folC | 2746752 | p.Gly283Cys | missense_variant | 0.17 |
folC | 2747282 | p.Glu106Gly | missense_variant | 0.11 |
pepQ | 2860075 | p.Glu115Gly | missense_variant | 0.2 |
ribD | 2987548 | p.Arg237Gln | missense_variant | 0.15 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474823 | p.Thr273Ala | missense_variant | 0.14 |
Rv3236c | 3612013 | c.1104A>T | synonymous_variant | 0.13 |
Rv3236c | 3612307 | p.Phe270Leu | missense_variant | 0.18 |
fbiB | 3641936 | c.402C>T | synonymous_variant | 0.12 |
fbiB | 3641960 | c.426C>A | synonymous_variant | 0.13 |
fbiB | 3642028 | p.Val165Asp | missense_variant | 0.22 |
ddn | 3987090 | p.Glu83Lys | missense_variant | 0.1 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038494 | c.2211G>A | synonymous_variant | 0.12 |
clpC1 | 4038732 | p.Lys658Arg | missense_variant | 0.12 |
clpC1 | 4039095 | c.1609delG | frameshift_variant | 0.12 |
clpC1 | 4039793 | c.912C>T | synonymous_variant | 0.12 |
clpC1 | 4040095 | c.608_609dupTG | frameshift_variant | 0.15 |
panD | 4044186 | c.95dupT | frameshift_variant | 0.25 |
embC | 4241276 | c.1414C>T | synonymous_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245968 | c.2738dupC | frameshift_variant | 0.15 |
embB | 4248378 | p.Ser622* | stop_gained | 0.14 |
embB | 4249609 | c.3098delA | frameshift_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408092 | c.111A>C | synonymous_variant | 0.17 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408162 | p.Pro14Leu | missense_variant | 0.12 |