Run ID: SRR4033258
Sample name:
Date: 04-04-2023 05:57:05
Number of reads: 1009935
Percentage reads mapped: 99.77
Strain: lineage4.8.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.97 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.95 |
lineage4.8.1 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.95 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8495 | c.1194C>T | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.16 |
mshA | 576036 | p.Ala230Val | missense_variant | 0.2 |
rpoC | 764359 | c.992_998delACGGCGG | frameshift_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.11 |
mmpL5 | 776505 | c.1975delC | frameshift_variant | 0.11 |
mmpL5 | 777660 | p.Ala274Val | missense_variant | 0.1 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417241 | p.Arg36Leu | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.86 |
inhA | 1674468 | c.271delG | frameshift_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102681 | p.Ala121Val | missense_variant | 0.1 |
katG | 2155182 | p.Lys310Asn | missense_variant | 0.12 |
katG | 2155254 | c.858C>A | synonymous_variant | 0.14 |
katG | 2155504 | p.Thr203Asn | missense_variant | 0.11 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 0.94 |
PPE35 | 2168590 | p.Gln675* | stop_gained | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2725954 | c.-239C>T | upstream_gene_variant | 0.14 |
folC | 2746623 | p.Val326Phe | missense_variant | 0.13 |
pepQ | 2859970 | p.Ala150Val | missense_variant | 0.14 |
Rv2752c | 3064969 | p.Lys408Arg | missense_variant | 0.11 |
fbiD | 3339040 | c.-78T>C | upstream_gene_variant | 0.92 |
whiB7 | 3568680 | c.-1C>T | upstream_gene_variant | 0.1 |
Rv3236c | 3612977 | p.Gly47Val | missense_variant | 0.11 |
fbiB | 3642874 | p.Leu447Arg | missense_variant | 0.94 |
ddn | 3986817 | c.-27C>T | upstream_gene_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243875 | p.Leu215Met | missense_variant | 0.1 |
embB | 4246746 | p.Asp78Gly | missense_variant | 0.1 |
ubiA | 4269696 | c.137delA | frameshift_variant | 0.14 |
ethA | 4326785 | p.Pro230Leu | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |