Run ID: ERR2513446
Sample name:
Date: 31-03-2023 19:41:03
Number of reads: 850101
Percentage reads mapped: 99.51
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.9 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.33 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.25 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.9 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.97 |
rpoC | 764359 | c.990C>A | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.95 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416290 | p.Gln353Arg | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471892 | n.47G>A | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.21 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.95 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168196 | p.Leu806Pro | missense_variant | 0.13 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.38 |
PPE35 | 2170232 | c.381T>A | synonymous_variant | 0.13 |
PPE35 | 2170238 | c.375T>G | synonymous_variant | 0.13 |
PPE35 | 2170247 | p.Ile122Met | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289692 | c.-451C>G | upstream_gene_variant | 0.11 |
pncA | 2290122 | c.-882dupG | upstream_gene_variant | 0.17 |
eis | 2715577 | c.-245G>A | upstream_gene_variant | 0.2 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ribD | 2987520 | p.Val228Leu | missense_variant | 0.18 |
thyX | 3067760 | c.186G>A | synonymous_variant | 0.12 |
thyA | 3073949 | p.Pro175Ala | missense_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474927 | c.921C>A | synonymous_variant | 0.11 |
Rv3236c | 3612217 | c.900C>T | synonymous_variant | 0.13 |
Rv3236c | 3612839 | p.Ala93Val | missense_variant | 0.17 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
panD | 4044037 | p.Gly82Val | missense_variant | 0.14 |
embC | 4240171 | c.309G>C | synonymous_variant | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embC | 4242172 | c.2310C>T | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242855 | p.Gly998Val | missense_variant | 0.12 |
embA | 4244184 | p.Ser318Leu | missense_variant | 0.13 |
embA | 4244966 | c.1734C>A | synonymous_variant | 0.15 |
embB | 4246816 | c.303C>T | synonymous_variant | 0.13 |
embB | 4248343 | c.1830G>T | synonymous_variant | 0.14 |
aftB | 4268808 | p.Val10Ala | missense_variant | 0.11 |
ethA | 4326406 | c.1068C>T | synonymous_variant | 1.0 |
ethA | 4326893 | p.Leu194Gln | missense_variant | 0.15 |
ethA | 4327139 | p.Ala112Gly | missense_variant | 1.0 |
ethA | 4327448 | p.Ile9Thr | missense_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |