Run ID: SRR3085283
Sample name:
Date: 04-04-2023 04:56:53
Number of reads: 905316
Percentage reads mapped: 99.31
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 | 7848 | p.Val183Phe | missense_variant | 0.13 |
gyrA | 9333 | p.Gly678Trp | missense_variant | 0.12 |
fgd1 | 490771 | c.-12T>G | upstream_gene_variant | 0.22 |
rpoB | 760021 | p.Gly72Val | missense_variant | 0.22 |
rpoB | 760711 | c.907delG | frameshift_variant | 0.17 |
rpoC | 763526 | p.Gly53Trp | missense_variant | 0.12 |
rpoC | 764972 | p.Asp535Tyr | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776580 | p.Leu634Gln | missense_variant | 0.15 |
mmpL5 | 777214 | p.Ala423Thr | missense_variant | 0.14 |
mmpL5 | 777747 | p.Gly245Val | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801062 | p.Arg85Gln | missense_variant | 0.17 |
rplC | 801133 | p.Gly109Cys | missense_variant | 0.15 |
fbiC | 1305449 | p.Ile840Asn | missense_variant | 0.12 |
embR | 1417066 | p.Leu94Phe | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473314 | n.1469A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473767 | n.110G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.91 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.13 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.14 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.1 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.1 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673585 | p.Ser49Tyr | missense_variant | 0.33 |
fabG1 | 1673840 | p.Arg134Leu | missense_variant | 0.14 |
inhA | 1674300 | c.99C>T | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102484 | p.Gly187* | stop_gained | 0.15 |
ndh | 2102616 | p.Asp143Tyr | missense_variant | 0.18 |
katG | 2154142 | p.Phe657Ser | missense_variant | 0.13 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.13 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.12 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 0.94 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.65 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.68 |
PPE35 | 2170302 | p.Met104Thr | missense_variant | 1.0 |
Rv1979c | 2222449 | p.Ala239Glu | missense_variant | 0.15 |
Rv1979c | 2222517 | c.648C>A | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517998 | c.-117C>A | upstream_gene_variant | 0.11 |
kasA | 2518147 | c.33C>T | synonymous_variant | 0.27 |
folC | 2746832 | p.Val256Gly | missense_variant | 0.18 |
pepQ | 2859437 | p.Val328Ile | missense_variant | 0.14 |
ribD | 2986847 | p.Asp3Glu | missense_variant | 0.14 |
Rv2752c | 3065868 | c.324C>A | synonymous_variant | 0.14 |
thyA | 3074331 | c.141C>A | synonymous_variant | 0.12 |
whiB7 | 3568831 | c.-152C>A | upstream_gene_variant | 0.15 |
fbiB | 3641634 | p.Ala34Ser | missense_variant | 0.13 |
clpC1 | 4040567 | c.138C>A | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242948 | p.Gly1029Val | missense_variant | 0.15 |
embC | 4243016 | p.Asp1052Tyr | missense_variant | 0.14 |
embA | 4243588 | p.Arg119Leu | missense_variant | 0.14 |
embA | 4245804 | p.Gln858* | stop_gained | 0.12 |
embA | 4246200 | p.Gln990Lys | missense_variant | 0.15 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.18 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.2 |
embB | 4246556 | p.Ala15Leu | missense_variant | 0.2 |
embB | 4248392 | p.Ala627Ser | missense_variant | 0.15 |
embB | 4249354 | c.2841G>C | synonymous_variant | 1.0 |
ubiA | 4268930 | p.Gly302Cys | missense_variant | 0.4 |
aftB | 4269246 | c.-410G>T | upstream_gene_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338598 | c.-77G>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |