Run ID: ERR2245348
Sample name:
Date: 31-03-2023 17:39:02
Number of reads: 2025871
Percentage reads mapped: 87.2
Strain: lineage3.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6290 | c.1054dupG | frameshift_variant | 0.2 |
gyrA | 6556 | c.-746C>T | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7623 | p.Pro108Ser | missense_variant | 0.15 |
gyrA | 8414 | c.1113C>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9383 | c.2082T>G | synonymous_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.3 |
mshA | 576676 | c.1329T>G | synonymous_variant | 0.18 |
ccsA | 620711 | p.Val274Gly | missense_variant | 0.14 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 759986 | c.180T>C | synonymous_variant | 0.1 |
rpoB | 760573 | c.769dupG | frameshift_variant | 0.13 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.88 |
rpoB | 762708 | p.Thr968Pro | missense_variant | 0.27 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764246 | p.Leu293Ile | missense_variant | 0.29 |
rpoC | 766326 | p.Gly986Val | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777191 | c.1290C>A | synonymous_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303396 | p.Arg156Gly | missense_variant | 0.12 |
fbiC | 1303670 | p.Asp247Ala | missense_variant | 0.27 |
Rv1258c | 1406248 | p.Leu365Val | missense_variant | 0.15 |
embR | 1416896 | p.Asp151Gly | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473635 | n.-23A>T | upstream_gene_variant | 0.29 |
rrl | 1475666 | n.2009T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673636 | p.Asp66Ala | missense_variant | 0.21 |
rpsA | 1833883 | c.342C>G | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155050 | c.1062C>T | synonymous_variant | 0.2 |
katG | 2156297 | c.-186T>G | upstream_gene_variant | 0.17 |
PPE35 | 2167916 | c.2696delT | frameshift_variant | 0.17 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169049 | p.Ile522Phe | missense_variant | 0.18 |
PPE35 | 2169063 | p.Met517Lys | missense_variant | 0.38 |
PPE35 | 2170082 | c.531T>G | synonymous_variant | 0.29 |
PPE35 | 2170119 | p.Leu165Arg | missense_variant | 0.17 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
Rv1979c | 2222393 | p.Ile258Phe | missense_variant | 0.13 |
Rv1979c | 2222657 | p.Lys170Glu | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289075 | p.Asp56Ala | missense_variant | 0.19 |
pncA | 2289301 | c.-60T>A | upstream_gene_variant | 0.12 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2519039 | p.Asn309Asp | missense_variant | 0.11 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ribD | 2986994 | c.156C>T | synonymous_variant | 0.12 |
Rv2752c | 3065092 | c.1099delC | frameshift_variant | 0.12 |
Rv2752c | 3065339 | p.Asp285Asn | missense_variant | 0.14 |
Rv2752c | 3065883 | c.309C>A | synonymous_variant | 0.29 |
thyX | 3067962 | c.-17G>T | upstream_gene_variant | 0.12 |
thyA | 3074204 | p.Leu90Ile | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087861 | p.Gly348Trp | missense_variant | 0.18 |
fbiD | 3339472 | p.Ala119Ser | missense_variant | 0.12 |
Rv3083 | 3449587 | p.Gly362Ser | missense_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474046 | p.Ser14Ala | missense_variant | 0.18 |
whiB7 | 3568489 | p.Gly64Ala | missense_variant | 0.12 |
Rv3236c | 3612593 | p.Asp175Val | missense_variant | 0.15 |
fbiB | 3641937 | p.Gly135Arg | missense_variant | 0.11 |
fbiB | 3642839 | c.1305G>A | synonymous_variant | 0.13 |
fbiB | 3642857 | c.1323C>A | synonymous_variant | 0.12 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.67 |
panD | 4044235 | p.Thr16Asn | missense_variant | 0.12 |
embC | 4239903 | c.42dupA | frameshift_variant | 0.14 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242683 | p.Thr941Ser | missense_variant | 0.2 |
embA | 4244550 | p.Ala440Thr | missense_variant | 0.17 |
embA | 4244745 | p.Leu505Val | missense_variant | 0.25 |
embA | 4245583 | p.Asp784Val | missense_variant | 0.13 |
embA | 4246206 | p.Pro992Ser | missense_variant | 0.14 |
embB | 4249134 | p.Leu874Pro | missense_variant | 0.14 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.29 |
ubiA | 4269354 | c.479delG | frameshift_variant | 0.18 |
ethA | 4328454 | c.-982delG | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407832 | p.Val124Ala | missense_variant | 0.12 |