Run ID: ERR2229174
Sample name:
Date: 31-03-2023 16:46:41
Number of reads: 1130592
Percentage reads mapped: 95.4
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 |
gyrA | 9327 | p.Ala676Thr | missense_variant | 0.13 |
mshA | 576043 | c.696G>T | synonymous_variant | 0.15 |
rpoB | 762697 | p.Ala964Asp | missense_variant | 0.17 |
rpoC | 767058 | p.Thr1230Asn | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.14 |
mmpL5 | 776021 | c.2460G>C | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474990 | n.1333C>A | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.3 |
fabG1 | 1673983 | c.548delC | frameshift_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101786 | c.1257G>T | synonymous_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169064 | p.Met517Leu | missense_variant | 0.13 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.18 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.16 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.39 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.45 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.2 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.12 |
kasA | 2519153 | p.Ile347Val | missense_variant | 0.15 |
eis | 2714275 | p.Arg353Leu | missense_variant | 0.17 |
folC | 2746290 | p.Arg437Cys | missense_variant | 0.22 |
folC | 2747459 | p.Leu47Pro | missense_variant | 0.11 |
pepQ | 2859557 | p.Glu288Lys | missense_variant | 0.13 |
thyX | 3068133 | c.-188G>A | upstream_gene_variant | 0.13 |
thyX | 3068139 | c.-194G>T | upstream_gene_variant | 0.15 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fprA | 3474663 | c.657C>T | synonymous_variant | 0.13 |
Rv3236c | 3612217 | c.900C>A | synonymous_variant | 0.18 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.23 |
clpC1 | 4038213 | p.Asp831Gly | missense_variant | 0.12 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.14 |
embC | 4242545 | p.Glu895* | stop_gained | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244212 | p.Pro327His | missense_variant | 0.2 |
embA | 4244683 | p.Arg484His | missense_variant | 0.12 |
embA | 4245551 | c.2322delC | frameshift_variant | 0.15 |
embA | 4245632 | p.Asn800Lys | missense_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.2 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.33 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.38 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.38 |
aftB | 4266967 | p.Pro624Thr | missense_variant | 0.13 |
ethR | 4326889 | c.-660C>T | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |