Run ID: SRR7851312
Sample name:
Date: 04-04-2023 20:22:49
Number of reads: 3252955
Percentage reads mapped: 87.49
Strain: La1.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.2 | M.bovis | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.34 | streptomycin |
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7475 | c.174A>G | synonymous_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7821 | c.520C>T | synonymous_variant | 1.0 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 8741 | c.1440C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575793 | p.Asp149Gly | missense_variant | 1.0 |
rpoB | 762197 | c.2391C>G | synonymous_variant | 0.11 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.12 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.14 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.14 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.16 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.16 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.13 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.1 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.14 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.14 |
rpoB | 763005 | p.Cys1067Gly | missense_variant | 0.11 |
rpoC | 763013 | c.-357C>A | upstream_gene_variant | 0.11 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.13 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763052 | c.-318G>T | upstream_gene_variant | 0.11 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.12 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.12 |
rpoC | 763106 | c.-264C>T | upstream_gene_variant | 0.13 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.13 |
rpoB | 763118 | p.Glu1104Asp | missense_variant | 0.12 |
rpoB | 763130 | p.Glu1108Asp | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.11 |
rpsL | 781817 | c.258G>C | synonymous_variant | 0.12 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.15 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.11 |
rpsL | 781860 | p.Ser101Ala | missense_variant | 0.11 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.1 |
rpsL | 781880 | c.321C>G | synonymous_variant | 0.11 |
rpsL | 781884 | p.Asn109Asp | missense_variant | 0.11 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471878 | n.33C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471925 | n.80T>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1471929 | n.84C>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1471931 | n.87_89delAGA | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472057 | n.212C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472671 | n.826G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472687 | n.842A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1473677 | n.20C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473697 | n.40C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473698 | n.41G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473699 | n.42A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473718 | n.61G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473728 | n.71A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473751 | n.94C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473752 | n.95G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474182 | n.525C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474183 | n.526T>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474904 | n.1247G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475525 | n.1868G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475539 | n.1882A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475769 | n.2112_2113insC | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475879 | n.2222T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475989 | n.2332T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475990 | n.2333G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476215 | n.2558_2559insTA | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476255 | n.2598A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476298 | n.2641C>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476309 | n.2652G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.16 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.17 |
rpsA | 1833422 | c.-120G>T | upstream_gene_variant | 1.0 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.11 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102106 | p.Gly313Arg | missense_variant | 0.99 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
katG | 2156465 | c.-354C>T | upstream_gene_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.42 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.41 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.17 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518654 | c.540C>T | synonymous_variant | 1.0 |
thyX | 3067786 | p.Thr54Ala | missense_variant | 1.0 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.3 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
fbiD | 3339154 | p.Ile13Leu | missense_variant | 1.0 |
Rv3083 | 3448745 | p.Ile81Ser | missense_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247173 | c.660G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |