Run ID: SRR6046115
Sample name:
Date: 04-04-2023 12:11:34
Number of reads: 588136
Percentage reads mapped: 65.23
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6932 | p.Gln565Lys | missense_variant | 0.17 |
gyrB | 7106 | p.Glu623Lys | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575424 | p.Arg26His | missense_variant | 1.0 |
mshA | 576089 | c.750_769delTGATCGGCGCGCGGCCCGGG | frameshift_variant | 0.25 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.3 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.35 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763321 | p.Ala1172Val | missense_variant | 0.12 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.13 |
mmpL5 | 776021 | c.2460G>C | synonymous_variant | 0.13 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777692 | c.789C>T | synonymous_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801229 | p.Ala141Pro | missense_variant | 0.18 |
fbiC | 1304136 | c.1206C>G | synonymous_variant | 0.33 |
fbiC | 1304524 | p.Ala532Thr | missense_variant | 0.22 |
fbiC | 1304694 | c.1764A>T | synonymous_variant | 0.12 |
Rv1258c | 1406235 | p.Pro369Gln | missense_variant | 0.12 |
embR | 1416781 | c.567A>C | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475879 | n.2222T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475897 | n.2240T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475900 | n.2243A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475937 | n.2280A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.4 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.33 |
rpsA | 1834025 | p.Gln162Lys | missense_variant | 0.14 |
rpsA | 1834180 | p.Lys213Asn | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918138 | p.Ala67Thr | missense_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167859 | c.2754T>G | synonymous_variant | 0.21 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289913 | c.-672T>C | upstream_gene_variant | 0.13 |
pncA | 2290147 | c.-906T>C | upstream_gene_variant | 0.25 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.33 |
folC | 2746212 | p.Arg463Gly | missense_variant | 0.12 |
folC | 2746525 | c.1074G>A | synonymous_variant | 0.17 |
folC | 2747689 | c.-91C>T | upstream_gene_variant | 0.18 |
ribD | 2986659 | c.-180G>A | upstream_gene_variant | 0.12 |
Rv2752c | 3064877 | p.Ser439Thr | missense_variant | 0.2 |
Rv2752c | 3065948 | p.Gly82Trp | missense_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473998 | c.-9G>A | upstream_gene_variant | 1.0 |
fprA | 3473998 | c.-10_-9insA | upstream_gene_variant | 1.0 |
fprA | 3474655 | p.Asp217His | missense_variant | 0.15 |
Rv3236c | 3612190 | c.927G>A | synonymous_variant | 0.15 |
fbiA | 3641426 | p.His295Arg | missense_variant | 0.11 |
fbiB | 3641766 | p.Ile78Val | missense_variant | 0.11 |
fbiB | 3642877 | p.Lys448Arg | missense_variant | 1.0 |
alr | 3840956 | c.465C>T | synonymous_variant | 0.12 |
clpC1 | 4040241 | p.Thr155Phe | missense_variant | 0.33 |
clpC1 | 4040249 | p.Glu152Gly | missense_variant | 0.29 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.13 |
embC | 4241077 | c.1215C>T | synonymous_variant | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244424 | p.Arg398Trp | missense_variant | 0.22 |
embA | 4245077 | c.1845G>C | synonymous_variant | 0.15 |
embB | 4247981 | c.1468C>T | synonymous_variant | 1.0 |
embB | 4248578 | p.Ala689Thr | missense_variant | 0.11 |
embB | 4248627 | p.Ala705Val | missense_variant | 0.13 |
aftB | 4267747 | p.Ser364Pro | missense_variant | 0.13 |
ethA | 4327472 | c.2T>C | start_lost | 0.13 |
ethA | 4328471 | c.-998A>G | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |