Run ID: ERR2229172
Sample name:
Date: 31-03-2023 16:46:41
Number of reads: 310267
Percentage reads mapped: 99.34
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5289 | p.Ile17Thr | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7932 | p.Asp211Asn | missense_variant | 0.33 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.29 |
mmpL5 | 775987 | p.His832Tyr | missense_variant | 0.33 |
mmpL5 | 775990 | c.2491C>T | synonymous_variant | 0.33 |
mmpL5 | 778278 | p.Ala68Glu | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302897 | c.-34G>T | upstream_gene_variant | 0.4 |
fbiC | 1305311 | p.Arg794Gln | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473948 | n.291C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833425 | c.-117C>G | upstream_gene_variant | 0.33 |
rpsA | 1833436 | c.-106C>T | upstream_gene_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154924 | c.1188C>A | synonymous_variant | 0.2 |
PPE35 | 2167773 | p.Gly947Val | missense_variant | 0.18 |
PPE35 | 2167833 | p.Leu927Arg | missense_variant | 0.25 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.18 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.17 |
PPE35 | 2168177 | c.2436T>A | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169365 | p.Ser416Asn | missense_variant | 0.14 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.22 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.22 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.53 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.56 |
PPE35 | 2170060 | p.Val185Leu | missense_variant | 0.22 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.2 |
Rv1979c | 2223048 | c.117G>T | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288909 | c.333G>A | synonymous_variant | 0.25 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.25 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.29 |
ribD | 2986877 | c.39G>T | synonymous_variant | 0.17 |
fbiD | 3339352 | p.Val79Ile | missense_variant | 0.2 |
fbiD | 3339370 | p.Pro85Ser | missense_variant | 0.29 |
fprA | 3474024 | c.18C>T | synonymous_variant | 0.22 |
fprA | 3474694 | p.Leu230Met | missense_variant | 0.33 |
Rv3236c | 3612791 | p.Trp109* | stop_gained | 0.15 |
rpoA | 3878340 | c.168C>A | synonymous_variant | 0.17 |
clpC1 | 4038773 | p.Asp644Glu | missense_variant | 0.5 |
clpC1 | 4038776 | p.Glu643Asp | missense_variant | 0.5 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.33 |
clpC1 | 4039594 | p.Arg371Gly | missense_variant | 0.2 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.22 |
clpC1 | 4040292 | p.Val138Glu | missense_variant | 0.29 |
clpC1 | 4040692 | p.Phe5Ile | missense_variant | 0.15 |
embC | 4239705 | c.-158T>C | upstream_gene_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243511 | c.279G>A | synonymous_variant | 0.29 |
embA | 4245494 | c.2262G>A | synonymous_variant | 0.4 |
embA | 4246182 | p.Ala984Thr | missense_variant | 0.29 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.6 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.71 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.71 |
embB | 4246563 | p.Leu17Trp | missense_variant | 1.0 |
embB | 4246567 | c.54G>T | synonymous_variant | 1.0 |
embB | 4247170 | c.657G>A | synonymous_variant | 0.14 |
aftB | 4267111 | c.1725delT | frameshift_variant | 0.2 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.14 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.14 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.14 |
ethR | 4327730 | p.Phe61Cys | missense_variant | 0.12 |
ethA | 4328289 | c.-816T>A | upstream_gene_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |