Run ID: SRR13837696
Sample name:
Date: 03-04-2023 09:16:07
Number of reads: 297264
Percentage reads mapped: 97.13
Strain: lineage4.9
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2154798 | c.1313_1314insT | frameshift_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5906 | p.Val223Leu | missense_variant | 1.0 |
gyrB | 6011 | p.Val258Met | missense_variant | 1.0 |
gyrB | 6678 | p.Pro480Arg | missense_variant | 1.0 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 0.17 |
gyrA | 7075 | c.-227T>C | upstream_gene_variant | 0.18 |
gyrA | 7078 | c.-224A>C | upstream_gene_variant | 0.2 |
gyrA | 7084 | c.-218A>G | upstream_gene_variant | 0.2 |
gyrA | 7090 | c.-212C>T | upstream_gene_variant | 0.2 |
gyrA | 7093 | c.-209T>G | upstream_gene_variant | 0.2 |
gyrA | 7099 | c.-203G>A | upstream_gene_variant | 0.2 |
fgd1 | 490676 | c.-107G>C | upstream_gene_variant | 1.0 |
ccsA | 620028 | c.138G>C | synonymous_variant | 1.0 |
rpoB | 759638 | c.-169T>A | upstream_gene_variant | 1.0 |
rpoB | 760454 | c.650delG | frameshift_variant | 1.0 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.15 |
rpoB | 762246 | c.2440C>T | synonymous_variant | 0.18 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.17 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.15 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.18 |
rpoC | 765487 | p.Met706Ile | missense_variant | 1.0 |
rpsL | 781409 | c.-151T>A | upstream_gene_variant | 1.0 |
fbiC | 1302873 | c.-58A>T | upstream_gene_variant | 1.0 |
rrs | 1471874 | n.29A>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476382 | n.2725A>T | non_coding_transcript_exon_variant | 0.33 |
rpsA | 1834123 | c.582C>G | synonymous_variant | 0.15 |
katG | 2154654 | p.Ser486Arg | missense_variant | 1.0 |
katG | 2154882 | c.1230G>A | synonymous_variant | 1.0 |
katG | 2155857 | c.255C>A | synonymous_variant | 1.0 |
PPE35 | 2170198 | p.Ala139Ser | missense_variant | 1.0 |
pncA | 2290069 | c.-828C>T | upstream_gene_variant | 1.0 |
eis | 2714922 | c.411G>A | synonymous_variant | 1.0 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.2 |
thyA | 3073874 | p.Ile200Val | missense_variant | 0.18 |
thyA | 3073917 | c.555C>G | synonymous_variant | 0.17 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.17 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.17 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.13 |
thyA | 3073941 | c.531C>T | synonymous_variant | 0.12 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.13 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.13 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.12 |
thyA | 3073983 | c.489C>T | synonymous_variant | 0.12 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.12 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.13 |
thyA | 3074028 | c.444G>C | synonymous_variant | 0.12 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.12 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.12 |
thyA | 3074067 | c.405C>G | synonymous_variant | 0.94 |
fbiB | 3641791 | p.Leu86Trp | missense_variant | 0.18 |
alr | 3840223 | c.1198A>C | synonymous_variant | 1.0 |
alr | 3840711 | p.Ser237Leu | missense_variant | 1.0 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.18 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.18 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.17 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.18 |
rpoA | 3878043 | c.465G>A | synonymous_variant | 0.18 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.2 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.2 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.2 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.18 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.18 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.2 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.18 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.18 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.17 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.15 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.17 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.2 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.15 |
rpoA | 3878143 | p.Gly122Asp | missense_variant | 0.15 |
clpC1 | 4038530 | c.2175G>A | synonymous_variant | 0.14 |
clpC1 | 4039648 | p.Glu353Gln | missense_variant | 0.9 |
embC | 4241530 | c.1668C>G | synonymous_variant | 0.14 |
embC | 4242023 | p.Val721Leu | missense_variant | 1.0 |
embA | 4245071 | c.1839G>A | synonymous_variant | 1.0 |
embB | 4249444 | c.2931T>C | synonymous_variant | 0.13 |
embB | 4249580 | p.Leu1023Met | missense_variant | 0.16 |
ethA | 4327364 | p.Lys37Arg | missense_variant | 1.0 |