Run ID: SRR6046779
Sample name:
Date: 04-04-2023 12:23:22
Number of reads: 2411593
Percentage reads mapped: 93.56
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.28 | streptomycin |
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 | 491027 | p.Asn82Thr | missense_variant | 0.31 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
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 |
rpsL | 781676 | c.117C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472813 | n.968A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472814 | n.969G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641843 | c.309G>A | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407986 | c.17_216del | frameshift_variant | 1.0 |