Run ID: SRR13861365
Sample name:
Date: 03-04-2023 09:29:59
Number of reads: 232986
Percentage reads mapped: 11.66
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
ethA | 4326568 | c.905delT | frameshift_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 8820 | p.Asp507His | missense_variant | 1.0 |
mshA | 575472 | p.Asp42Ala | missense_variant | 0.2 |
mshA | 575967 | p.Val207Asp | missense_variant | 1.0 |
rpoB | 759961 | p.Thr52Asn | missense_variant | 1.0 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.22 |
rpoB | 763050 | p.Leu1082Met | missense_variant | 1.0 |
mmpL5 | 775701 | p.Pro927Gln | missense_variant | 1.0 |
mmpL5 | 778828 | c.-348G>A | upstream_gene_variant | 1.0 |
rplC | 801353 | p.Val182Ala | missense_variant | 1.0 |
fbiC | 1304512 | p.Val528Ile | missense_variant | 1.0 |
rrs | 1472936 | n.1091C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472971 | n.1126G>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473051 | n.1206T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473053 | n.1208T>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.15 |
rpsA | 1834175 | p.Arg212* | stop_gained | 1.0 |
Rv1979c | 2222085 | c.1080G>C | synonymous_variant | 1.0 |
folC | 2746135 | c.1464A>C | stop_lost&splice_region_variant | 1.0 |
ald | 3087218 | p.Met133Ile | missense_variant | 1.0 |
whiB7 | 3568679 | p.Val1Leu | missense_variant | 1.0 |
clpC1 | 4040066 | c.639G>T | synonymous_variant | 1.0 |
embC | 4241259 | c.1397_1398insT | frameshift_variant | 1.0 |
embA | 4243358 | c.126C>T | synonymous_variant | 1.0 |
embA | 4243469 | c.237C>T | synonymous_variant | 1.0 |
embB | 4248436 | c.1923C>T | synonymous_variant | 1.0 |
ubiA | 4269557 | p.Ala93Pro | missense_variant | 1.0 |