Run ID: SRR6046151
Sample name:
Date: 04-04-2023 12:12:01
Number of reads: 5678
Percentage reads mapped: 7.33
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 |
---|---|---|---|---|
rpoB | 760274 | c.468G>A | synonymous_variant | 1.0 |
rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
rpoB | 760313 | c.507G>C | synonymous_variant | 1.0 |
rpoB | 760316 | c.510C>G | synonymous_variant | 1.0 |
rpoB | 760325 | c.519G>C | synonymous_variant | 1.0 |
rpoB | 760328 | c.522G>C | synonymous_variant | 1.0 |
rpoB | 760331 | c.525G>T | synonymous_variant | 1.0 |
rpoB | 760340 | c.534G>T | synonymous_variant | 1.0 |
rpoB | 760634 | c.828T>C | synonymous_variant | 1.0 |
rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
rpoB | 760649 | c.843G>C | synonymous_variant | 1.0 |
rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
rpoB | 760661 | c.855A>C | synonymous_variant | 1.0 |
rpoB | 760670 | c.864G>C | synonymous_variant | 1.0 |
rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
rpoB | 761984 | c.2178G>A | synonymous_variant | 1.0 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 1.0 |
rpoB | 762000 | c.2194_2195delTCinsAG | synonymous_variant | 1.0 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 1.0 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 1.0 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 1.0 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 1.0 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 1.0 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 1.0 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 1.0 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
rpoC | 763082 | c.-288C>G | upstream_gene_variant | 1.0 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 1.0 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 1.0 |
rpoC | 763160 | c.-210G>T | upstream_gene_variant | 1.0 |
rpoC | 765405 | p.Leu679Arg | missense_variant | 1.0 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 1.0 |
rpoC | 765454 | c.2085C>G | synonymous_variant | 1.0 |
rpoC | 765466 | c.2097C>T | synonymous_variant | 1.0 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 1.0 |
rpoC | 765499 | c.2130C>A | synonymous_variant | 1.0 |
rpoC | 765533 | p.Tyr722His | missense_variant | 1.0 |
rpoC | 766321 | c.2952C>G | synonymous_variant | 1.0 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 1.0 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 1.0 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 1.0 |
mmpL5 | 776027 | c.2454G>C | synonymous_variant | 1.0 |
mmpL5 | 776039 | c.2442C>A | synonymous_variant | 1.0 |
rplC | 800678 | c.-131C>T | upstream_gene_variant | 1.0 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
rpsA | 1833892 | c.351G>A | synonymous_variant | 1.0 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 1.0 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 1.0 |
rpsA | 1833994 | c.453G>A | synonymous_variant | 1.0 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 1.0 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 1.0 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 1.0 |
rpsA | 1834408 | c.867C>G | synonymous_variant | 1.0 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
rpsA | 1834414 | c.873C>T | synonymous_variant | 1.0 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 1.0 |
katG | 2155632 | c.480A>C | synonymous_variant | 1.0 |
katG | 2155635 | c.477C>T | synonymous_variant | 1.0 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 1.0 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 1.0 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 1.0 |
rpoA | 3877671 | c.837C>G | synonymous_variant | 1.0 |
rpoA | 3877677 | c.831G>C | synonymous_variant | 1.0 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 1.0 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 1.0 |
clpC1 | 4038578 | c.2127C>T | synonymous_variant | 1.0 |
clpC1 | 4038587 | c.2118C>T | synonymous_variant | 1.0 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
clpC1 | 4038605 | c.2100G>A | synonymous_variant | 1.0 |
clpC1 | 4038613 | p.Asn698His | missense_variant | 1.0 |
clpC1 | 4038614 | c.2091C>T | synonymous_variant | 1.0 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 1.0 |
clpC1 | 4039592 | c.1113G>C | synonymous_variant | 1.0 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 1.0 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 1.0 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 1.0 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 1.0 |
clpC1 | 4039670 | c.1035G>C | synonymous_variant | 1.0 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 1.0 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 1.0 |
clpC1 | 4039942 | c.763C>T | synonymous_variant | 1.0 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 1.0 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 1.0 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 1.0 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
clpC1 | 4040456 | c.249C>G | synonymous_variant | 1.0 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
clpC1 | 4040468 | c.237G>C | synonymous_variant | 1.0 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
clpC1 | 4040501 | c.204C>G | synonymous_variant | 1.0 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 1.0 |
clpC1 | 4040644 | c.61A>C | synonymous_variant | 1.0 |
clpC1 | 4040654 | c.51G>A | synonymous_variant | 1.0 |
clpC1 | 4040669 | c.36C>T | synonymous_variant | 1.0 |
clpC1 | 4040674 | c.31A>C | synonymous_variant | 1.0 |
clpC1 | 4040675 | c.30C>T | synonymous_variant | 1.0 |
clpC1 | 4040678 | c.27C>A | synonymous_variant | 1.0 |
clpC1 | 4040690 | c.15T>C | synonymous_variant | 1.0 |
clpC1 | 4040695 | c.10C>A | synonymous_variant | 1.0 |
embC | 4240819 | c.957A>C | synonymous_variant | 1.0 |
embC | 4240831 | c.969T>G | synonymous_variant | 1.0 |
embC | 4240852 | c.990G>C | synonymous_variant | 1.0 |
embC | 4240855 | c.993G>T | synonymous_variant | 1.0 |
embC | 4240867 | c.1005T>G | synonymous_variant | 1.0 |
embC | 4240870 | c.1008T>C | synonymous_variant | 1.0 |