Run ID: ERR2229444
Sample name:
Date: 31-03-2023 17:11:52
Number of reads: 730129
Percentage reads mapped: 98.85
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 |
---|---|---|---|---|
gyrB | 6747 | p.Gln503Arg | missense_variant | 0.17 |
gyrB | 6771 | p.Thr511Ile | missense_variant | 0.17 |
gyrB | 7120 | c.1884delC | frameshift_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8626 | p.Arg442His | missense_variant | 0.14 |
gyrA | 8822 | p.Asp507Glu | missense_variant | 0.18 |
mshA | 575265 | c.-83C>A | upstream_gene_variant | 0.18 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.29 |
mshA | 576547 | p.Asp400Glu | missense_variant | 0.17 |
mshA | 576616 | c.1269G>A | synonymous_variant | 0.11 |
rpoC | 766798 | c.3429C>A | synonymous_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775822 | p.Val887Leu | missense_variant | 0.13 |
mmpL5 | 776196 | p.Ala762Glu | missense_variant | 0.12 |
mmpL5 | 776221 | p.Ser754Pro | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800779 | c.-30T>C | upstream_gene_variant | 0.15 |
rplC | 800983 | p.Pro59Gln | missense_variant | 0.14 |
fbiC | 1303444 | c.516dupC | frameshift_variant | 0.18 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406429 | c.912C>G | synonymous_variant | 0.11 |
atpE | 1461043 | c.-2A>G | upstream_gene_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473043 | n.1202dupC | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474740 | n.1083G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474940 | n.1283C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475573 | n.1921delC | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.43 |
rpsA | 1834218 | p.Val226Ala | missense_variant | 0.12 |
tlyA | 1917876 | c.-64C>A | upstream_gene_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101708 | c.1335G>T | synonymous_variant | 0.15 |
ndh | 2103001 | c.42G>A | synonymous_variant | 0.14 |
katG | 2155810 | p.Leu101Gln | missense_variant | 0.22 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168809 | p.Val602Ile | missense_variant | 0.12 |
PPE35 | 2169215 | p.Glu466Asp | missense_variant | 0.12 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.45 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.5 |
Rv1979c | 2222797 | p.Pro123Leu | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518230 | p.Gly39Val | missense_variant | 0.12 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.25 |
eis | 2714771 | p.Gly188Cys | missense_variant | 0.14 |
ahpC | 2726470 | c.281delT | frameshift_variant | 0.15 |
pepQ | 2860373 | p.Ala16Thr | missense_variant | 0.15 |
thyA | 3074272 | p.Ser67Tyr | missense_variant | 0.12 |
ald | 3086852 | p.Asn11Lys | missense_variant | 0.15 |
Rv3083 | 3448481 | c.-23G>T | upstream_gene_variant | 0.33 |
fprA | 3474038 | p.Ser11Tyr | missense_variant | 0.12 |
whiB7 | 3568626 | c.53delT | frameshift_variant | 0.12 |
Rv3236c | 3612618 | p.Pro167Ser | missense_variant | 0.18 |
Rv3236c | 3612881 | p.Ala79Val | missense_variant | 0.18 |
Rv3236c | 3613183 | c.-67C>A | upstream_gene_variant | 0.22 |
fbiB | 3641190 | c.-345G>C | upstream_gene_variant | 0.12 |
fbiB | 3642639 | p.Glu369* | stop_gained | 0.18 |
fbiB | 3642695 | c.1161G>A | synonymous_variant | 0.29 |
rpoA | 3878166 | c.342C>G | synonymous_variant | 0.18 |
ddn | 3986693 | c.-150delG | upstream_gene_variant | 0.15 |
ddn | 3986711 | c.-133C>T | upstream_gene_variant | 0.15 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.16 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.22 |
clpC1 | 4040359 | c.344_345delAG | frameshift_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246154 | c.-360G>A | upstream_gene_variant | 0.4 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.2 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.47 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.54 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.54 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.29 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.29 |
embB | 4246747 | p.Asp78Glu | missense_variant | 0.18 |
embB | 4247153 | p.Pro214Ser | missense_variant | 0.2 |
embB | 4247176 | c.663G>C | synonymous_variant | 0.15 |
embB | 4249378 | c.2865G>T | synonymous_variant | 0.12 |
embB | 4249682 | c.3172delG | frameshift_variant | 0.25 |
aftB | 4268529 | p.Gly103Asp | missense_variant | 0.15 |
ubiA | 4268974 | p.Leu287Gln | missense_variant | 0.15 |
ethA | 4327281 | p.Arg65* | stop_gained | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |