Run ID: SRR15315871
Sample name:
Date: 03-04-2023 12:55:06
Number of reads: 314249
Percentage reads mapped: 4.0
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.89 |
rpoB | 762870 | p.Met1022Val | missense_variant | 0.9 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.91 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.91 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.93 |
rpoB | 762925 | p.Thr1040Ile | missense_variant | 0.89 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.89 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.89 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.89 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.83 |
rpoC | 762983 | c.-387C>A | upstream_gene_variant | 0.93 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.87 |
rpoC | 762998 | c.-372G>A | upstream_gene_variant | 0.87 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.8 |
rpoC | 763013 | c.-357C>T | upstream_gene_variant | 0.75 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.75 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.75 |
rpoC | 763022 | c.-348C>T | upstream_gene_variant | 0.75 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.75 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764857 | c.1488G>C | synonymous_variant | 1.0 |
rpoC | 764858 | p.Leu497Met | missense_variant | 1.0 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 1.0 |
rpoC | 764872 | c.1503A>T | synonymous_variant | 1.0 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 1.0 |
rpoC | 764887 | c.1518G>A | synonymous_variant | 1.0 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 1.0 |
rpoC | 764911 | c.1542A>C | synonymous_variant | 1.0 |
rpoC | 764914 | p.Met515Ile | missense_variant | 1.0 |
rpoC | 764918 | p.Val517Ile | missense_variant | 1.0 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
rpoC | 764948 | c.1579_1581delTTGinsCTC | synonymous_variant | 1.0 |
rpoC | 764953 | c.1584G>C | synonymous_variant | 1.0 |
rpoC | 764956 | c.1587T>C | synonymous_variant | 1.0 |
rpoC | 764958 | p.Glu530Ala | missense_variant | 1.0 |
rpoC | 764962 | c.1593G>C | synonymous_variant | 1.0 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
rpoC | 764995 | c.1626C>T | synonymous_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
fbiC | 1303906 | p.Gly326Cys | missense_variant | 1.0 |
rrs | 1471892 | n.47G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471898 | n.53A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472135 | n.290C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472181 | n.336G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472349 | n.504A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472374 | n.529T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472390 | n.545T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472415 | n.570T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472936 | n.1091C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473051 | n.1206T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476022 | n.2365A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476025 | n.2368G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476238 | n.2581T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476266 | n.2609G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476279 | n.2622G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476281 | n.2624T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476339 | n.2682G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476356 | n.2699C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476384 | n.2727G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476521 | n.2864C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476584 | n.2927C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476588 | n.2931A>T | non_coding_transcript_exon_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2859830 | p.Gly197Trp | missense_variant | 1.0 |
rpoA | 3878390 | p.Arg40Cys | missense_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |