Run ID: ERR2228821
Sample name:
Date: 31-03-2023 16:22:03
Number of reads: 784995
Percentage reads mapped: 99.36
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576330 | p.Leu328Gln | missense_variant | 0.23 |
rpoC | 766892 | p.Phe1175Leu | missense_variant | 0.22 |
rpoC | 766910 | p.Ile1181Leu | missense_variant | 0.33 |
rpoC | 766914 | p.Asp1182Ala | missense_variant | 0.22 |
rpoC | 766938 | p.Asn1190Ile | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776027 | c.2454G>A | synonymous_variant | 0.14 |
mmpL5 | 776030 | c.2451G>A | synonymous_variant | 0.14 |
mmpL5 | 776751 | p.Phe577Ser | missense_variant | 0.17 |
mmpL5 | 778919 | c.-439A>T | upstream_gene_variant | 0.44 |
mmpR5 | 779125 | p.Cys46Arg | missense_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801077 | p.Asp90Gly | missense_variant | 0.12 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304216 | p.Asn429Thr | missense_variant | 0.25 |
fbiC | 1304981 | p.Lys684Met | missense_variant | 0.33 |
atpE | 1461143 | p.Asn33Lys | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473885 | n.228A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475388 | n.1731A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475567 | n.1914delA | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673329 | c.-111A>C | upstream_gene_variant | 0.27 |
fabG1 | 1673642 | p.Val68Gly | missense_variant | 0.22 |
fabG1 | 1674006 | p.Asp189Glu | missense_variant | 0.33 |
inhA | 1674356 | p.Asp52Ala | missense_variant | 0.33 |
inhA | 1674371 | p.Lys57Thr | missense_variant | 0.4 |
inhA | 1674400 | p.Asn67Tyr | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918453 | p.Ser172Ala | missense_variant | 0.12 |
ndh | 2102411 | p.Val211Gly | missense_variant | 0.14 |
ndh | 2102471 | p.Glu191Ala | missense_variant | 0.16 |
katG | 2155660 | p.Val151Gly | missense_variant | 0.19 |
PPE35 | 2168586 | p.Ile676Asn | missense_variant | 0.2 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169017 | p.Leu532Phe | missense_variant | 0.21 |
PPE35 | 2169031 | p.Asp528Tyr | missense_variant | 0.18 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.13 |
PPE35 | 2170436 | c.177T>G | synonymous_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289826 | c.-585A>T | upstream_gene_variant | 0.2 |
kasA | 2518605 | p.Val164Gly | missense_variant | 0.17 |
folC | 2746281 | p.Ile440Phe | missense_variant | 0.18 |
folC | 2746331 | p.Glu423Ala | missense_variant | 0.22 |
folC | 2747056 | p.Trp181Cys | missense_variant | 0.25 |
pepQ | 2859490 | p.Val310Gly | missense_variant | 0.31 |
pepQ | 2860101 | c.318C>A | synonymous_variant | 0.14 |
Rv2752c | 3064717 | p.Leu492Gln | missense_variant | 0.67 |
Rv2752c | 3065638 | p.Leu185Gln | missense_variant | 0.25 |
ald | 3087763 | p.Asn315Thr | missense_variant | 0.28 |
fbiD | 3339253 | p.Thr46Ser | missense_variant | 0.27 |
fbiD | 3339422 | p.Val102Glu | missense_variant | 0.4 |
fprA | 3474769 | p.Tyr255Asp | missense_variant | 0.12 |
Rv3236c | 3612569 | p.Val183Gly | missense_variant | 0.6 |
Rv3236c | 3612862 | p.Ser85Arg | missense_variant | 0.21 |
fbiB | 3641857 | p.Val108Gly | missense_variant | 0.27 |
fbiB | 3642837 | p.Leu435Val | missense_variant | 0.14 |
alr | 3840384 | p.Phe346Ser | missense_variant | 0.13 |
alr | 3840588 | p.Lys278Ile | missense_variant | 0.17 |
rpoA | 3878040 | c.468T>A | synonymous_variant | 0.25 |
rpoA | 3878490 | c.18C>G | synonymous_variant | 0.4 |
clpC1 | 4040031 | p.Val225Gly | missense_variant | 0.19 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242645 | p.Asn928Thr | missense_variant | 0.31 |
embA | 4244817 | p.Phe529Ile | missense_variant | 0.5 |
embA | 4245568 | p.Glu779Ala | missense_variant | 0.29 |
embA | 4245655 | p.Asp808Ala | missense_variant | 0.4 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.12 |
aftB | 4267756 | p.Lys361* | stop_gained | 0.25 |
ubiA | 4268986 | p.Val283Gly | missense_variant | 0.14 |
ubiA | 4269043 | p.Val264Gly | missense_variant | 0.27 |
ethA | 4327365 | p.Lys37* | stop_gained | 0.17 |
ethR | 4328104 | p.Ser186Ala | missense_variant | 0.23 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |