Run ID: ERR400529
Sample name:
Date: 01-04-2023 03:52:19
Number of reads: 2644039
Percentage reads mapped: 82.81
Strain: lineage3
Drug-resistance: Other
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 |
---|---|---|---|---|
gyrA | 7165 | c.-137C>T | upstream_gene_variant | 0.13 |
gyrA | 7168 | c.-134C>G | upstream_gene_variant | 0.14 |
gyrA | 7198 | c.-104C>T | upstream_gene_variant | 0.16 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.15 |
gyrA | 9033 | c.1732C>A | synonymous_variant | 0.9 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491232 | c.450T>C | synonymous_variant | 0.13 |
fgd1 | 491283 | p.Asp167Glu | missense_variant | 0.17 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.17 |
fgd1 | 491316 | c.534C>G | synonymous_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620757 | c.867C>T | synonymous_variant | 0.13 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.2 |
ccsA | 620787 | c.897C>G | synonymous_variant | 0.22 |
ccsA | 620793 | c.903G>C | synonymous_variant | 0.2 |
ccsA | 620808 | c.918T>C | synonymous_variant | 0.2 |
ccsA | 620832 | c.942C>G | synonymous_variant | 0.13 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.14 |
rpoB | 760118 | c.312T>C | synonymous_variant | 0.17 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.17 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.19 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.18 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.17 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.13 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.14 |
rpoB | 760313 | c.507G>C | synonymous_variant | 0.13 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.15 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.16 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.14 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.16 |
rpoB | 760451 | c.645C>G | synonymous_variant | 0.13 |
rpoB | 760463 | c.657C>T | synonymous_variant | 0.14 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.18 |
rpoB | 760643 | c.837G>A | synonymous_variant | 0.16 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.16 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.14 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.14 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.15 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.14 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.14 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.14 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.15 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762813 | p.Met1003Val | missense_variant | 0.16 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.16 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.15 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.15 |
rpoC | 763822 | c.453C>G | synonymous_variant | 0.16 |
rpoC | 763825 | c.456G>A | synonymous_variant | 0.15 |
rpoC | 763828 | c.459C>G | synonymous_variant | 0.16 |
rpoC | 763836 | p.Ala156Val | missense_variant | 0.15 |
rpoC | 764188 | c.819A>G | synonymous_variant | 0.17 |
rpoC | 764195 | p.Ser276Asn | missense_variant | 0.16 |
rpoC | 764203 | c.834G>T | synonymous_variant | 0.16 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 0.16 |
rpoC | 764209 | c.840C>T | synonymous_variant | 0.16 |
rpoC | 764217 | p.Asn283Ser | missense_variant | 0.17 |
rpoC | 764227 | c.858G>C | synonymous_variant | 0.17 |
rpoC | 764245 | c.876C>T | synonymous_variant | 0.18 |
rpoC | 764359 | c.990C>T | synonymous_variant | 0.13 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.13 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.16 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.17 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.17 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.14 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.13 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.15 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.14 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.19 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.17 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.15 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.17 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.18 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.18 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.14 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.22 |
rpoC | 765356 | p.Met663Val | missense_variant | 0.12 |
rpoC | 765370 | c.2001G>C | synonymous_variant | 0.15 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.16 |
rpoC | 765394 | c.2025G>A | synonymous_variant | 0.14 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.16 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.16 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.18 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.13 |
rpoC | 765547 | c.2178C>A | synonymous_variant | 0.14 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.14 |
rpoC | 765619 | c.2250G>A | synonymous_variant | 0.13 |
rpoC | 765676 | c.2307G>A | synonymous_variant | 0.14 |
rpoC | 765688 | c.2319G>C | synonymous_variant | 0.16 |
rpoC | 765694 | c.2325G>C | synonymous_variant | 0.16 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.13 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.14 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.13 |
rpoC | 765865 | c.2496C>T | synonymous_variant | 0.15 |
rpoC | 765871 | c.2502T>C | synonymous_variant | 0.16 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.18 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.15 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.15 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.15 |
rpoC | 765946 | c.2577C>T | synonymous_variant | 0.15 |
rpoC | 766342 | c.2973C>T | synonymous_variant | 0.17 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.16 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.16 |
rpoC | 766480 | c.3111C>G | synonymous_variant | 0.13 |
rpoC | 766484 | p.Val1039Ile | missense_variant | 0.13 |
rpoC | 766495 | c.3126C>G | synonymous_variant | 0.18 |
rpoC | 766522 | c.3153C>T | synonymous_variant | 0.19 |
rpoC | 766525 | c.3156G>T | synonymous_variant | 0.2 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.19 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.2 |
rpoC | 766558 | c.3189G>A | synonymous_variant | 0.2 |
rpoC | 766564 | c.3195C>T | synonymous_variant | 0.15 |
rpoC | 766565 | p.Ile1066Val | missense_variant | 0.15 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.17 |
rpoC | 766585 | c.3216T>C | synonymous_variant | 0.21 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.17 |
rpoC | 766618 | c.3249G>T | synonymous_variant | 0.15 |
rpoC | 766624 | c.3255G>C | synonymous_variant | 0.14 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.15 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.15 |
rpoC | 766667 | p.Ser1100Ala | missense_variant | 0.18 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.17 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.19 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 0.21 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.21 |
rpoC | 766753 | c.3384C>T | synonymous_variant | 0.23 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.23 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.21 |
rpoC | 766798 | c.3429C>T | synonymous_variant | 0.16 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.16 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 0.14 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.13 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.13 |
rpoC | 766960 | c.3591C>T | synonymous_variant | 0.13 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.14 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.15 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.13 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.13 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.13 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.15 |
rpoC | 767152 | c.3783T>G | synonymous_variant | 0.19 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 0.17 |
rpoC | 767167 | c.3798C>T | synonymous_variant | 0.19 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.17 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.17 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.14 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.14 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.15 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.16 |
rpoC | 767239 | c.3870T>C | synonymous_variant | 0.14 |
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 | 781649 | c.90T>C | synonymous_variant | 0.14 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.13 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.13 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.14 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.13 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.15 |
rplC | 800690 | c.-119C>G | upstream_gene_variant | 0.18 |
rplC | 800703 | c.-106_-104delTTGinsCTC | upstream_gene_variant | 0.15 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.15 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.17 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.16 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.22 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.2 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.19 |
rplC | 800829 | c.21C>G | synonymous_variant | 0.13 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.13 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.15 |
fbiC | 1303584 | c.654C>G | synonymous_variant | 0.2 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.2 |
fbiC | 1303614 | c.684C>G | synonymous_variant | 0.2 |
fbiC | 1303623 | c.693C>T | synonymous_variant | 0.18 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.16 |
fbiC | 1303641 | c.711C>T | synonymous_variant | 0.16 |
fbiC | 1303650 | c.720G>C | synonymous_variant | 0.15 |
fbiC | 1303654 | c.724C>T | synonymous_variant | 0.18 |
fbiC | 1303661 | p.Val244Ala | missense_variant | 0.15 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.16 |
fbiC | 1303704 | c.774T>G | synonymous_variant | 0.15 |
fbiC | 1303713 | c.783C>G | synonymous_variant | 0.15 |
fbiC | 1303722 | c.792C>T | synonymous_variant | 0.18 |
fbiC | 1303731 | c.801A>G | synonymous_variant | 0.16 |
fbiC | 1303732 | p.Ser268Ala | missense_variant | 0.16 |
fbiC | 1303740 | c.810C>G | synonymous_variant | 0.15 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 0.15 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.14 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 0.16 |
fbiC | 1303791 | c.861C>T | synonymous_variant | 0.16 |
fbiC | 1303794 | c.864A>G | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1471984 | n.139T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472314 | n.469A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472315 | n.470T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473814 | n.157A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473831 | n.174G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474029 | n.372G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474716 | n.1059A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475061 | n.1404C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475337 | n.1680C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475369 | n.1712G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475403 | n.1746T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475404 | n.1747A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475604 | n.1947A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475619 | n.1962C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475622 | n.1965G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475635 | n.1978G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475637 | n.1980T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475988 | n.2331A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476095 | n.2438C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.19 |
inhA | 1673991 | c.-211C>T | upstream_gene_variant | 0.14 |
inhA | 1674015 | c.-187C>G | upstream_gene_variant | 0.13 |
rpsA | 1833664 | c.123C>A | synonymous_variant | 0.13 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.18 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.17 |
rpsA | 1833817 | c.276C>G | synonymous_variant | 0.18 |
rpsA | 1833820 | c.279G>A | synonymous_variant | 0.19 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.14 |
rpsA | 1833859 | c.318C>T | synonymous_variant | 0.14 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.12 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.13 |
rpsA | 1834123 | c.582C>G | synonymous_variant | 0.15 |
rpsA | 1834189 | c.648G>C | synonymous_variant | 0.14 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.13 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.15 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.18 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.16 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.18 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.2 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.13 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.15 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.17 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.16 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.21 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.2 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.21 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.21 |
rpsA | 1834477 | c.936C>A | synonymous_variant | 0.19 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.17 |
rpsA | 1834499 | c.958C>T | synonymous_variant | 0.15 |
rpsA | 1834507 | c.966C>T | synonymous_variant | 0.13 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.13 |
rpsA | 1834534 | c.993C>G | synonymous_variant | 0.14 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.15 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.14 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.13 |
rpsA | 1834654 | c.1113G>A | synonymous_variant | 0.15 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.16 |
rpsA | 1834669 | c.1128G>C | synonymous_variant | 0.16 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.17 |
Rv1979c | 2222460 | c.704delT | frameshift_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.13 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339567 | c.450A>G | synonymous_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3640560 | c.-975G>A | upstream_gene_variant | 0.96 |
rpoA | 3877569 | c.939G>C | synonymous_variant | 0.13 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.14 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.14 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.13 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.15 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.16 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.16 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.18 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.2 |
rpoA | 3878130 | c.378C>G | synonymous_variant | 0.2 |
rpoA | 3878141 | c.365_366delGC | frameshift_variant | 0.19 |
rpoA | 3878145 | c.362_363insGT | frameshift_variant | 0.2 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.13 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 0.17 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.14 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.16 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.17 |
rpoA | 3878406 | c.102G>T | synonymous_variant | 0.21 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.24 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 0.16 |
rpoA | 3878454 | c.54A>G | synonymous_variant | 0.16 |
rpoA | 3878458 | p.Asn17Ser | missense_variant | 0.13 |
rpoA | 3878460 | c.48C>T | synonymous_variant | 0.12 |
clpC1 | 4038236 | p.Thr823Ala | missense_variant | 0.15 |
clpC1 | 4038239 | c.2466T>A | synonymous_variant | 0.17 |
clpC1 | 4038266 | c.2439C>T | synonymous_variant | 0.15 |
clpC1 | 4038270 | p.Pro812Ser | missense_variant | 0.14 |
clpC1 | 4038272 | c.2433T>C | synonymous_variant | 0.14 |
clpC1 | 4038275 | c.2430A>G | synonymous_variant | 0.17 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.17 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.14 |
clpC1 | 4038761 | c.1944C>T | synonymous_variant | 0.13 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.15 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.19 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.22 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.22 |
clpC1 | 4038838 | c.1867C>T | synonymous_variant | 0.17 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.18 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.17 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.16 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.16 |
clpC1 | 4039010 | c.1695G>C | synonymous_variant | 0.17 |
clpC1 | 4039076 | c.1629G>A | synonymous_variant | 0.21 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.12 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.14 |
clpC1 | 4039124 | c.1581C>G | synonymous_variant | 0.14 |
clpC1 | 4039140 | p.Glu522Val | missense_variant | 0.15 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.15 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.16 |
clpC1 | 4039370 | c.1335G>A | synonymous_variant | 0.15 |
clpC1 | 4039382 | c.1323C>T | synonymous_variant | 0.15 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.13 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.16 |
clpC1 | 4039439 | c.1266C>T | synonymous_variant | 0.17 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.18 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.25 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.25 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.27 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.3 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.29 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.27 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.26 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.25 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.25 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.15 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.13 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.13 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.15 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.15 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.16 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.17 |
clpC1 | 4039985 | c.720G>A | synonymous_variant | 0.19 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.2 |
clpC1 | 4040015 | c.690G>T | synonymous_variant | 0.19 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.18 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.2 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.19 |
embC | 4240765 | c.903C>G | synonymous_variant | 0.15 |
embC | 4240777 | c.915G>A | synonymous_variant | 0.16 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.16 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.16 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.17 |
embC | 4240795 | c.933C>G | synonymous_variant | 0.18 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.17 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.17 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.97 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245128 | c.1896G>C | synonymous_variant | 0.14 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.14 |
embA | 4245167 | c.1935G>C | synonymous_variant | 0.13 |
embB | 4248185 | c.1672T>C | synonymous_variant | 0.13 |
embB | 4248305 | c.1792C>T | synonymous_variant | 0.21 |
embB | 4248316 | c.1803C>G | synonymous_variant | 0.21 |
embB | 4248319 | c.1806A>G | synonymous_variant | 0.18 |
embB | 4248322 | c.1809G>T | synonymous_variant | 0.18 |
embB | 4248334 | c.1821C>G | synonymous_variant | 0.18 |
embB | 4248338 | c.1825C>T | synonymous_variant | 0.17 |
embB | 4249276 | c.2763A>C | synonymous_variant | 0.16 |
embB | 4249282 | c.2769A>C | synonymous_variant | 0.15 |
embB | 4249321 | c.2808A>G | synonymous_variant | 0.19 |
embB | 4249323 | p.Ala937Asp | missense_variant | 0.19 |
embB | 4249339 | c.2826T>C | synonymous_variant | 0.17 |
embB | 4249369 | c.2856T>C | synonymous_variant | 0.16 |
embB | 4249376 | c.2863C>T | synonymous_variant | 0.18 |
embB | 4249381 | c.2868A>G | synonymous_variant | 0.19 |
embB | 4249396 | c.2883C>T | synonymous_variant | 0.18 |
embB | 4249429 | c.2916C>G | synonymous_variant | 0.14 |
ubiA | 4269903 | c.-70C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |