Run ID: SRR21677870
Sample name:
Date: 04-04-2023 02:49:00
Number of reads: 119027
Percentage reads mapped: 93.47
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6927 | p.Leu563Ser | missense_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7370 | p.Glu23Asp | missense_variant | 0.33 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9439 | p.Ser713* | stop_gained | 0.4 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576439 | c.1092G>A | synonymous_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763539 | p.Asp57Gly | missense_variant | 0.22 |
rpoC | 766944 | p.Arg1192Gln | missense_variant | 0.17 |
rpoC | 767140 | c.3771G>C | synonymous_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777183 | c.1297delG | frameshift_variant | 0.33 |
mmpL5 | 778263 | p.Ile73Asn | missense_variant | 0.33 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304898 | c.1968G>T | synonymous_variant | 0.67 |
Rv1258c | 1406089 | p.Ala418Ser | missense_variant | 1.0 |
Rv1258c | 1406619 | p.Pro241Gln | missense_variant | 0.5 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461000 | c.-45C>T | upstream_gene_variant | 0.2 |
atpE | 1461064 | p.Ala7Val | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472430 | n.585C>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472444 | n.599A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472493 | n.649delA | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473451 | n.-207G>A | upstream_gene_variant | 0.29 |
rrl | 1473958 | n.303delT | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474092 | n.435G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475030 | n.1373G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476100 | n.2443A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476116 | n.2459A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673782 | p.Gly115Trp | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101810 | c.1233C>A | synonymous_variant | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2168439 | p.Ser725Phe | missense_variant | 0.33 |
PPE35 | 2170786 | c.-175delT | upstream_gene_variant | 0.4 |
Rv1979c | 2221800 | c.1365G>A | synonymous_variant | 0.4 |
Rv1979c | 2222057 | p.Asp370Asn | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289085 | p.Asp53Tyr | missense_variant | 0.4 |
kasA | 2518722 | c.610delG | frameshift_variant | 0.5 |
kasA | 2519104 | c.990T>A | synonymous_variant | 0.67 |
eis | 2715046 | p.Leu96Trp | missense_variant | 0.4 |
folC | 2747746 | c.-149delC | upstream_gene_variant | 0.33 |
pepQ | 2859524 | c.894delT | frameshift_variant | 0.67 |
ribD | 2987221 | p.Arg128His | missense_variant | 0.29 |
Rv2752c | 3065596 | p.Leu199Ser | missense_variant | 0.5 |
Rv2752c | 3066036 | p.His52Gln | missense_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087819 | c.1000C>A | synonymous_variant | 0.29 |
ald | 3087834 | c.1016delT | frameshift_variant | 0.33 |
Rv3083 | 3449397 | c.894C>T | synonymous_variant | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474831 | c.825G>T | synonymous_variant | 0.33 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640975 | p.Ala145Ser | missense_variant | 0.22 |
alr | 3840739 | c.682C>A | synonymous_variant | 0.4 |
rpoA | 3878259 | c.249G>T | synonymous_variant | 0.4 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 1.0 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243801 | p.Asp190Val | missense_variant | 0.4 |
embB | 4247330 | p.Trp273Arg | missense_variant | 0.29 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4269693 | c.-857C>T | upstream_gene_variant | 1.0 |
ethA | 4326185 | p.Pro430Arg | missense_variant | 0.15 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 1.0 |
ethR | 4327670 | p.Pro41Gln | missense_variant | 1.0 |
ethA | 4328246 | c.-773C>T | upstream_gene_variant | 0.18 |
ethA | 4328421 | c.-948G>T | upstream_gene_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407651 | c.552T>C | synonymous_variant | 0.33 |
gid | 4407878 | p.Gly109Arg | missense_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |