Run ID: SRR13837684
Sample name:
Date: 03-04-2023 09:15:51
Number of reads: 296593
Percentage reads mapped: 97.91
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 |
---|---|---|---|---|
gyrB | 5192 | c.-48C>G | upstream_gene_variant | 1.0 |
gyrB | 6136 | c.897G>A | synonymous_variant | 0.12 |
gyrB | 6148 | c.909C>G | synonymous_variant | 0.11 |
gyrB | 6169 | c.930C>G | synonymous_variant | 0.12 |
gyrB | 6190 | c.951A>G | synonymous_variant | 0.12 |
gyrB | 6209 | c.970C>T | synonymous_variant | 0.12 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.12 |
gyrB | 6217 | c.978G>C | synonymous_variant | 0.13 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.19 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.15 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.17 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.17 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.18 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.18 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.18 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.2 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.2 |
gyrB | 6299 | c.1060C>T | synonymous_variant | 0.2 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.2 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.22 |
gyrA | 6325 | c.-977C>G | upstream_gene_variant | 0.25 |
gyrA | 6361 | c.-941G>A | upstream_gene_variant | 0.29 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.29 |
gyrA | 9658 | c.2357_2358insT | frameshift_variant | 1.0 |
fgd1 | 490779 | c.-4A>T | upstream_gene_variant | 1.0 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.13 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.14 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.14 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.2 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.2 |
mshA | 575752 | c.405G>A | synonymous_variant | 0.12 |
mshA | 575767 | c.420G>A | synonymous_variant | 0.15 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.14 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.14 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.12 |
rpoB | 760041 | p.Gly79Arg | missense_variant | 1.0 |
rpoB | 760652 | c.846C>A | synonymous_variant | 0.92 |
rpoB | 761122 | p.Pro439Arg | missense_variant | 1.0 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.22 |
mmpL5 | 775929 | p.Asn851Ile | missense_variant | 1.0 |
mmpS5 | 778941 | c.-36A>G | upstream_gene_variant | 1.0 |
rplC | 801324 | c.516T>C | synonymous_variant | 0.15 |
fbiC | 1303584 | c.654C>G | synonymous_variant | 0.29 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.33 |
fbiC | 1303602 | c.672A>G | synonymous_variant | 0.33 |
fbiC | 1303605 | c.675C>G | synonymous_variant | 0.33 |
fbiC | 1303608 | c.678G>A | synonymous_variant | 0.33 |
fbiC | 1303611 | c.681G>C | synonymous_variant | 0.33 |
fbiC | 1303614 | c.684C>T | synonymous_variant | 0.33 |
fbiC | 1303617 | c.687C>G | synonymous_variant | 0.33 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.33 |
fbiC | 1303638 | c.708A>G | synonymous_variant | 0.33 |
fbiC | 1303653 | c.723G>C | synonymous_variant | 0.33 |
fbiC | 1303659 | c.729T>C | synonymous_variant | 0.33 |
fbiC | 1303660 | p.Val244Thr | missense_variant | 0.33 |
fbiC | 1303674 | c.744C>G | synonymous_variant | 0.33 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 0.33 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.43 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.29 |
fbiC | 1303728 | c.798G>A | synonymous_variant | 0.33 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.18 |
embR | 1417376 | c.-29T>C | upstream_gene_variant | 1.0 |
rrl | 1473740 | n.83G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474574 | n.917A>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834610 | p.Arg357Gly | missense_variant | 1.0 |
ndh | 2101828 | c.1215C>T | synonymous_variant | 1.0 |
PPE35 | 2168706 | p.Ser636Phe | missense_variant | 1.0 |
pncA | 2289887 | c.-646A>C | upstream_gene_variant | 1.0 |
folC | 2746838 | p.Ala254Glu | missense_variant | 1.0 |
ribD | 2987500 | p.Gly221Asp | missense_variant | 1.0 |
thyX | 3068082 | c.-137T>C | upstream_gene_variant | 1.0 |
fbiD | 3338954 | c.-164A>G | upstream_gene_variant | 1.0 |
fbiD | 3339235 | p.Leu40Val | missense_variant | 1.0 |
fbiD | 3339406 | p.Thr97Ala | missense_variant | 1.0 |
Rv3083 | 3448625 | p.Leu41Gln | missense_variant | 1.0 |
fbiB | 3642247 | p.Asn238Thr | missense_variant | 1.0 |
fbiB | 3642283 | p.Glu250Ala | missense_variant | 1.0 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.11 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.11 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.12 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.14 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.14 |
clpC1 | 4039483 | c.1221_1222insC | frameshift_variant | 1.0 |
embA | 4243843 | c.613dupG | frameshift_variant | 1.0 |
embA | 4244833 | p.Val534Ala | missense_variant | 1.0 |
embA | 4245735 | p.Ala835Ser | missense_variant | 1.0 |
aftB | 4267994 | p.Met281Ile | missense_variant | 1.0 |