Run ID: SRR5535697
Sample name:
Date: 04-04-2023 10:38:02
Number of reads: 1469171
Percentage reads mapped: 99.19
Strain: lineage4.1.2
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 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
katG | 2155666 | p.Trp149* | stop_gained | 0.25 | isoniazid |
embC | 4240676 | p.Gly272Ser | missense_variant | 0.18 | ethambutol |
ethA | 4326278 | p.Ser399* | stop_gained | 1.0 | ethionamide |
gid | 4407686 | p.Glu173* | stop_gained | 0.29 | streptomycin |
gid | 4407985 | p.Gly73Ala | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5698 | c.459G>T | synonymous_variant | 0.33 |
gyrB | 5797 | c.558C>T | synonymous_variant | 0.18 |
gyrB | 6470 | p.Val411Leu | missense_variant | 0.2 |
gyrB | 6539 | p.Asp434Tyr | missense_variant | 0.22 |
gyrB | 7031 | p.Gly598Trp | missense_variant | 0.67 |
gyrB | 7127 | p.Val630Phe | missense_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7802 | c.501C>A | synonymous_variant | 0.18 |
gyrA | 7818 | p.Leu173Met | missense_variant | 0.14 |
gyrA | 8223 | p.Asp308Asn | missense_variant | 0.18 |
gyrA | 8675 | c.1374C>A | synonymous_variant | 0.2 |
gyrA | 9239 | c.1938C>T | synonymous_variant | 0.33 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9684 | p.Gly795* | stop_gained | 0.5 |
fgd1 | 491522 | p.Arg247Gln | missense_variant | 0.33 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575350 | c.3G>T | start_lost | 0.38 |
mshA | 575421 | p.Thr25Asn | missense_variant | 0.14 |
mshA | 575431 | c.84C>A | synonymous_variant | 0.15 |
mshA | 575449 | c.102C>A | synonymous_variant | 0.17 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 575728 | c.381C>A | synonymous_variant | 0.22 |
mshA | 575743 | p.Phe132Leu | missense_variant | 0.29 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.15 |
mshA | 576308 | p.Ile321Val | missense_variant | 0.2 |
mshA | 576318 | p.Arg324Leu | missense_variant | 0.2 |
mshA | 576776 | p.Gly477Arg | missense_variant | 0.2 |
ccsA | 619713 | c.-178C>A | upstream_gene_variant | 0.17 |
ccsA | 619716 | c.-175G>T | upstream_gene_variant | 0.27 |
ccsA | 619723 | c.-168G>T | upstream_gene_variant | 0.18 |
ccsA | 619724 | c.-167C>A | upstream_gene_variant | 0.18 |
ccsA | 619756 | c.-135G>A | upstream_gene_variant | 0.2 |
ccsA | 620323 | p.Val145Met | missense_variant | 0.67 |
rpoB | 759742 | c.-65G>T | upstream_gene_variant | 0.4 |
rpoB | 760520 | c.714C>A | synonymous_variant | 0.25 |
rpoB | 760536 | p.Glu244* | stop_gained | 0.2 |
rpoB | 760539 | p.Arg245Trp | missense_variant | 0.2 |
rpoB | 760564 | p.Arg253Leu | missense_variant | 0.25 |
rpoB | 760569 | p.Thr255Pro | missense_variant | 0.25 |
rpoB | 760688 | p.Phe294Leu | missense_variant | 0.33 |
rpoB | 760697 | p.Glu297Asp | missense_variant | 0.33 |
rpoB | 761000 | p.Met398Ile | missense_variant | 0.5 |
rpoB | 761298 | p.Ala498Thr | missense_variant | 0.4 |
rpoB | 761338 | p.Arg511His | missense_variant | 0.4 |
rpoB | 761610 | p.Gly602Trp | missense_variant | 0.4 |
rpoB | 761613 | p.Ala603Ser | missense_variant | 0.4 |
rpoB | 762831 | p.Ser1009Arg | missense_variant | 0.4 |
rpoC | 763187 | c.-183C>A | upstream_gene_variant | 0.67 |
rpoC | 763582 | p.Lys71Asn | missense_variant | 0.25 |
rpoC | 764057 | p.Ala230Ser | missense_variant | 0.25 |
rpoC | 764810 | p.Pro481Thr | missense_variant | 0.27 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.9 |
rpoC | 765291 | p.Arg641Leu | missense_variant | 0.25 |
rpoC | 765402 | p.Pro678Gln | missense_variant | 0.25 |
rpoC | 765450 | p.Ala694Asp | missense_variant | 0.25 |
rpoC | 765544 | c.2175C>A | synonymous_variant | 0.22 |
rpoC | 765564 | p.Ser732* | stop_gained | 0.25 |
rpoC | 765572 | p.Asp735Tyr | missense_variant | 0.25 |
rpoC | 765598 | p.Lys743Asn | missense_variant | 0.5 |
rpoC | 765638 | p.Glu757Lys | missense_variant | 0.29 |
rpoC | 765664 | p.Leu765Phe | missense_variant | 0.29 |
rpoC | 765849 | p.Pro827Gln | missense_variant | 0.17 |
rpoC | 765932 | p.Gly855Cys | missense_variant | 0.25 |
rpoC | 766617 | p.Arg1083Leu | missense_variant | 0.67 |
rpoC | 767149 | c.3780C>T | synonymous_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775674 | p.Trp936Leu | missense_variant | 0.17 |
mmpL5 | 775716 | p.Arg922Gln | missense_variant | 0.25 |
mmpL5 | 775973 | c.2508G>A | synonymous_variant | 1.0 |
mmpL5 | 776169 | p.Gly771Val | missense_variant | 0.5 |
mmpL5 | 776759 | p.Phe574Leu | missense_variant | 0.5 |
mmpL5 | 777310 | p.Gly391Cys | missense_variant | 0.25 |
mmpL5 | 777319 | p.Arg388Ser | missense_variant | 0.2 |
mmpS5 | 778484 | p.Ser141Tyr | missense_variant | 0.18 |
mmpL5 | 778585 | c.-105C>T | upstream_gene_variant | 0.22 |
mmpS5 | 778857 | p.Val17Met | missense_variant | 0.4 |
mmpR5 | 779254 | p.Arg89Trp | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781406 | c.-154G>T | upstream_gene_variant | 0.33 |
rplC | 800689 | c.-120G>A | upstream_gene_variant | 0.25 |
rplC | 800860 | p.Asp18Asn | missense_variant | 0.18 |
rplC | 800922 | c.114C>A | synonymous_variant | 0.18 |
rplC | 801078 | c.270T>C | synonymous_variant | 0.13 |
fbiC | 1302766 | c.-165C>A | upstream_gene_variant | 0.22 |
fbiC | 1303452 | c.522G>T | synonymous_variant | 0.18 |
fbiC | 1303690 | p.Pro254Thr | missense_variant | 0.67 |
fbiC | 1304800 | p.Arg624Trp | missense_variant | 0.67 |
fbiC | 1304862 | p.Lys644Asn | missense_variant | 0.4 |
fbiC | 1305152 | p.Pro741Gln | missense_variant | 0.2 |
fbiC | 1305265 | p.Gly779Arg | missense_variant | 0.22 |
fbiC | 1305463 | p.Arg845Ser | missense_variant | 0.15 |
Rv1258c | 1406120 | c.1221C>A | synonymous_variant | 0.17 |
Rv1258c | 1406294 | c.1047C>A | synonymous_variant | 0.2 |
Rv1258c | 1407426 | c.-86C>A | upstream_gene_variant | 0.29 |
embR | 1416253 | c.1095C>T | synonymous_variant | 0.22 |
embR | 1416369 | p.Arg327Ser | missense_variant | 0.3 |
embR | 1416435 | p.Ala305Ser | missense_variant | 0.18 |
embR | 1416718 | p.Gln210His | missense_variant | 0.18 |
embR | 1417031 | p.Pro106His | missense_variant | 0.5 |
embR | 1417194 | p.Val52Phe | missense_variant | 0.4 |
rrs | 1471771 | n.-75C>A | upstream_gene_variant | 1.0 |
rrs | 1473090 | n.1245G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473404 | n.-254C>A | upstream_gene_variant | 0.4 |
rrl | 1474503 | n.846G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475313 | n.1656G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476427 | n.2770G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476781 | n.3124C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476787 | n.3130C>A | non_coding_transcript_exon_variant | 0.5 |
fabG1 | 1673912 | p.Ala158Val | missense_variant | 0.5 |
fabG1 | 1674085 | p.Glu216* | stop_gained | 0.67 |
fabG1 | 1674155 | c.719_721delACG | disruptive_inframe_deletion | 0.4 |
inhA | 1674312 | c.111G>A | synonymous_variant | 0.29 |
inhA | 1674329 | p.Arg43Leu | missense_variant | 0.29 |
inhA | 1674423 | p.Leu74Phe | missense_variant | 0.33 |
inhA | 1674775 | p.Gly192Cys | missense_variant | 0.25 |
inhA | 1674954 | c.753G>A | synonymous_variant | 0.22 |
rpsA | 1833775 | p.Glu78Asp | missense_variant | 0.29 |
rpsA | 1834093 | c.552G>T | synonymous_variant | 0.2 |
rpsA | 1834466 | p.Ala309Ser | missense_variant | 0.6 |
rpsA | 1834519 | c.978G>T | synonymous_variant | 0.22 |
rpsA | 1834876 | c.1335G>T | synonymous_variant | 0.25 |
tlyA | 1917792 | c.-148G>T | upstream_gene_variant | 0.2 |
tlyA | 1917800 | c.-140A>C | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918387 | p.Leu150Met | missense_variant | 0.17 |
tlyA | 1918737 | p.Glu266Asp | missense_variant | 0.29 |
tlyA | 1918742 | p.Pro268Gln | missense_variant | 0.29 |
ndh | 2101942 | p.Lys367Asn | missense_variant | 0.22 |
ndh | 2101965 | p.Glu360* | stop_gained | 0.25 |
ndh | 2101975 | c.1068G>T | synonymous_variant | 0.22 |
ndh | 2102244 | p.Arg267Trp | missense_variant | 0.22 |
ndh | 2102813 | p.Arg77His | missense_variant | 0.25 |
katG | 2153907 | c.2205C>T | synonymous_variant | 0.22 |
katG | 2154035 | p.Arg693Ser | missense_variant | 0.29 |
katG | 2154183 | c.1929G>T | synonymous_variant | 0.33 |
katG | 2154584 | p.Pro510Thr | missense_variant | 0.15 |
katG | 2154910 | p.Pro401His | missense_variant | 0.22 |
katG | 2154933 | c.1179C>A | synonymous_variant | 0.25 |
katG | 2155020 | c.1092C>T | synonymous_variant | 0.2 |
katG | 2155030 | p.Ala361Val | missense_variant | 0.25 |
katG | 2155259 | p.Gly285Cys | missense_variant | 0.67 |
katG | 2155572 | c.540G>A | synonymous_variant | 0.29 |
katG | 2156469 | c.-358G>T | upstream_gene_variant | 0.25 |
PPE35 | 2167910 | c.2703C>A | synonymous_variant | 0.29 |
PPE35 | 2168917 | p.Pro566Thr | missense_variant | 0.33 |
PPE35 | 2170073 | p.Ala180Ser | missense_variant | 0.2 |
PPE35 | 2170132 | p.Val161Ile | missense_variant | 0.25 |
PPE35 | 2170139 | c.474G>A | synonymous_variant | 0.25 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.22 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.2 |
PPE35 | 2170222 | p.Pro131Thr | missense_variant | 0.18 |
PPE35 | 2170319 | p.Glu98Asp | missense_variant | 0.2 |
PPE35 | 2170628 | c.-16C>A | upstream_gene_variant | 0.67 |
PPE35 | 2170761 | c.-149G>T | upstream_gene_variant | 0.5 |
Rv1979c | 2222085 | c.1080G>A | synonymous_variant | 0.29 |
Rv1979c | 2222155 | p.Pro337Gln | missense_variant | 0.22 |
Rv1979c | 2222451 | c.714C>A | synonymous_variant | 0.33 |
Rv1979c | 2222501 | p.Ala222Thr | missense_variant | 1.0 |
Rv1979c | 2222519 | p.Gly216Cys | missense_variant | 0.29 |
Rv1979c | 2223156 | c.9C>A | synonymous_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223297 | c.-133G>T | upstream_gene_variant | 0.4 |
pncA | 2289134 | c.108C>A | synonymous_variant | 0.29 |
pncA | 2289873 | c.-632C>A | upstream_gene_variant | 0.4 |
pncA | 2290021 | c.-780C>A | upstream_gene_variant | 0.33 |
pncA | 2290147 | c.-906T>C | upstream_gene_variant | 0.5 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518152 | p.Ser13Ile | missense_variant | 0.22 |
kasA | 2518438 | p.Phe108Leu | missense_variant | 0.22 |
kasA | 2518530 | p.Pro139Gln | missense_variant | 0.29 |
kasA | 2518832 | p.Gly240Cys | missense_variant | 0.18 |
kasA | 2518849 | c.735G>T | synonymous_variant | 0.25 |
kasA | 2518909 | p.Leu265Phe | missense_variant | 0.25 |
kasA | 2518912 | c.798G>T | synonymous_variant | 0.25 |
kasA | 2519144 | p.Gly344Cys | missense_variant | 0.17 |
kasA | 2519343 | p.Ala410Val | missense_variant | 0.2 |
eis | 2714160 | c.1173C>G | synonymous_variant | 0.29 |
eis | 2714370 | c.963C>A | synonymous_variant | 0.22 |
eis | 2715195 | c.138G>T | synonymous_variant | 0.18 |
eis | 2715282 | p.Phe17Leu | missense_variant | 0.17 |
eis | 2715409 | c.-77C>A | upstream_gene_variant | 0.29 |
ahpC | 2726541 | p.Glu117* | stop_gained | 0.4 |
ahpC | 2726611 | p.Pro140His | missense_variant | 0.4 |
ahpC | 2726763 | p.Leu191Ile | missense_variant | 0.33 |
folC | 2746166 | p.Ala478Asp | missense_variant | 0.33 |
folC | 2746387 | c.1212C>A | synonymous_variant | 0.25 |
folC | 2746494 | p.Glu369* | stop_gained | 0.27 |
folC | 2746843 | c.756C>A | synonymous_variant | 0.29 |
folC | 2747185 | c.414G>T | synonymous_variant | 0.18 |
folC | 2747496 | p.Asp35Tyr | missense_variant | 0.22 |
folC | 2747679 | c.-81C>A | upstream_gene_variant | 0.4 |
pepQ | 2859535 | p.Gly295Val | missense_variant | 0.29 |
pepQ | 2859701 | p.Gly240Cys | missense_variant | 0.25 |
pepQ | 2860281 | p.Phe46Leu | missense_variant | 0.25 |
ribD | 2986818 | c.-21C>T | upstream_gene_variant | 0.22 |
ribD | 2986917 | p.Glu27* | stop_gained | 0.33 |
ribD | 2986925 | c.87C>G | synonymous_variant | 0.29 |
ribD | 2986985 | p.Leu49Phe | missense_variant | 0.22 |
Rv2752c | 3064661 | p.Val511Leu | missense_variant | 0.25 |
Rv2752c | 3065460 | c.732G>T | synonymous_variant | 0.25 |
Rv2752c | 3066029 | p.Pro55Ser | missense_variant | 0.5 |
Rv2752c | 3066125 | p.Gly23Ser | missense_variant | 0.33 |
Rv2752c | 3066319 | c.-128T>G | upstream_gene_variant | 0.33 |
thyX | 3067634 | c.312C>A | synonymous_variant | 0.4 |
thyX | 3067790 | c.156C>A | synonymous_variant | 0.17 |
thyA | 3073833 | c.639C>A | synonymous_variant | 0.5 |
thyA | 3073964 | p.Leu170Met | missense_variant | 0.25 |
thyA | 3073976 | p.Arg166Ser | missense_variant | 0.25 |
thyA | 3074153 | p.Glu107* | stop_gained | 0.22 |
thyA | 3074216 | p.Asp86Tyr | missense_variant | 0.5 |
thyA | 3074436 | c.36C>A | synonymous_variant | 0.5 |
ald | 3086649 | c.-171C>A | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086825 | c.6C>T | synonymous_variant | 0.33 |
ald | 3087399 | p.Val194Ile | missense_variant | 0.2 |
ald | 3087725 | c.906C>A | synonymous_variant | 0.19 |
Rv3083 | 3449411 | p.Gly303Val | missense_variant | 0.15 |
Rv3083 | 3449442 | c.939G>A | synonymous_variant | 0.18 |
Rv3083 | 3449621 | p.Tyr373Cys | missense_variant | 0.2 |
fprA | 3473984 | c.-23G>T | upstream_gene_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474276 | c.270C>A | synonymous_variant | 0.5 |
fprA | 3474753 | c.747C>A | synonymous_variant | 0.18 |
fprA | 3474934 | p.Arg310Ser | missense_variant | 0.2 |
fprA | 3475098 | c.1092G>T | synonymous_variant | 0.22 |
whiB7 | 3568403 | c.277T>C | stop_lost&splice_region_variant | 0.2 |
whiB7 | 3568533 | p.Arg49Ser | missense_variant | 0.18 |
whiB7 | 3568675 | p.Ser2* | stop_gained | 0.67 |
whiB7 | 3568758 | c.-79C>A | upstream_gene_variant | 0.2 |
Rv3236c | 3612069 | p.Gly350Trp | missense_variant | 1.0 |
Rv3236c | 3612103 | p.Leu338Phe | missense_variant | 0.5 |
fbiB | 3640593 | c.-942C>A | upstream_gene_variant | 0.25 |
fbiA | 3640621 | p.Gln27Lys | missense_variant | 0.22 |
fbiB | 3640755 | c.-780C>A | upstream_gene_variant | 0.18 |
fbiA | 3640766 | p.Pro75His | missense_variant | 0.17 |
fbiA | 3640876 | p.His112Asn | missense_variant | 0.29 |
fbiA | 3641378 | p.Arg279Leu | missense_variant | 0.25 |
fbiB | 3641543 | c.9C>A | synonymous_variant | 0.29 |
fbiB | 3642575 | c.1041C>A | synonymous_variant | 0.31 |
alr | 3840272 | c.1149C>A | synonymous_variant | 0.18 |
alr | 3840920 | c.501G>T | synonymous_variant | 0.29 |
alr | 3841006 | p.Asp139Tyr | missense_variant | 0.22 |
alr | 3841029 | p.Ala131Val | missense_variant | 0.2 |
alr | 3841293 | p.Gly43Val | missense_variant | 0.25 |
alr | 3841295 | c.126G>T | synonymous_variant | 0.29 |
alr | 3841375 | p.Asp16Asn | missense_variant | 0.33 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.67 |
rpoA | 3878041 | p.Gly156Val | missense_variant | 0.29 |
rpoA | 3878060 | p.Val150Met | missense_variant | 0.4 |
rpoA | 3878359 | p.Ala50Asp | missense_variant | 0.67 |
ddn | 3986700 | c.-144C>A | upstream_gene_variant | 0.15 |
ddn | 3986738 | c.-106C>A | upstream_gene_variant | 0.22 |
clpC1 | 4038408 | p.Pro766Gln | missense_variant | 0.6 |
clpC1 | 4038767 | c.1938G>T | synonymous_variant | 0.17 |
clpC1 | 4039244 | c.1461G>T | synonymous_variant | 0.17 |
clpC1 | 4039678 | p.Gln343* | stop_gained | 1.0 |
clpC1 | 4039954 | p.Asp251Asn | missense_variant | 0.25 |
clpC1 | 4040669 | c.36C>G | synonymous_variant | 0.5 |
clpC1 | 4040722 | c.-18G>T | upstream_gene_variant | 0.29 |
embC | 4239672 | c.-191G>A | upstream_gene_variant | 0.22 |
embC | 4239950 | p.Arg30Trp | missense_variant | 0.18 |
embC | 4240004 | p.Pro48Thr | missense_variant | 0.22 |
embC | 4240306 | c.444C>A | synonymous_variant | 0.22 |
embC | 4240850 | p.Leu330Met | missense_variant | 0.15 |
embC | 4241010 | p.Gly383Asp | missense_variant | 0.17 |
embC | 4241706 | p.Ser615* | stop_gained | 0.5 |
embC | 4242139 | c.2277G>A | synonymous_variant | 0.25 |
embC | 4242344 | p.Ala828Thr | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242649 | c.-584G>A | upstream_gene_variant | 0.18 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243865 | c.633G>T | synonymous_variant | 0.15 |
embA | 4243886 | p.Met218Ile | missense_variant | 0.2 |
embA | 4243966 | p.Arg245Leu | missense_variant | 0.27 |
embA | 4244159 | c.927G>T | synonymous_variant | 0.33 |
embA | 4244214 | p.Ala328Thr | missense_variant | 0.2 |
embA | 4244587 | p.Leu452Pro | missense_variant | 0.13 |
embA | 4244614 | p.Ala461Val | missense_variant | 0.17 |
embA | 4245404 | c.2172C>A | synonymous_variant | 0.25 |
embB | 4245791 | c.-723C>A | upstream_gene_variant | 0.25 |
embA | 4245822 | p.Pro864Ser | missense_variant | 0.2 |
embB | 4245905 | c.-609C>A | upstream_gene_variant | 0.22 |
embB | 4246232 | c.-282C>A | upstream_gene_variant | 0.67 |
embB | 4246660 | c.147C>A | synonymous_variant | 0.18 |
embB | 4246686 | p.Trp58* | stop_gained | 0.18 |
embB | 4247239 | p.Leu242Phe | missense_variant | 0.29 |
embB | 4247981 | p.Leu490Met | missense_variant | 0.25 |
embB | 4248392 | p.Ala627Ser | missense_variant | 0.5 |
embB | 4248536 | p.Leu675Met | missense_variant | 0.17 |
aftB | 4267384 | p.Ala485Ser | missense_variant | 0.25 |
aftB | 4267669 | p.Ala390Thr | missense_variant | 0.29 |
aftB | 4268150 | p.Met229Ile | missense_variant | 0.5 |
aftB | 4268187 | p.Gly217Val | missense_variant | 1.0 |
aftB | 4268731 | p.Arg36Trp | missense_variant | 0.33 |
aftB | 4268747 | c.90C>T | synonymous_variant | 0.5 |
aftB | 4268887 | c.-51C>A | upstream_gene_variant | 0.2 |
ubiA | 4269449 | p.Val129Phe | missense_variant | 0.14 |
ubiA | 4269491 | p.Ala115Ser | missense_variant | 0.15 |
aftB | 4269651 | c.-815G>A | upstream_gene_variant | 0.25 |
ethA | 4326011 | p.Gly488Val | missense_variant | 0.25 |
ethA | 4326065 | p.Arg470His | missense_variant | 0.25 |
ethA | 4326168 | p.Pro436Thr | missense_variant | 0.33 |
ethA | 4326190 | p.Glu428Asp | missense_variant | 0.15 |
ethR | 4326982 | c.-567C>T | upstream_gene_variant | 0.25 |
ethA | 4327028 | p.Pro149Gln | missense_variant | 0.25 |
ethR | 4327444 | c.-105C>A | upstream_gene_variant | 0.33 |
ethA | 4327458 | p.Asp6Tyr | missense_variant | 0.29 |
ethA | 4327608 | c.-135C>T | upstream_gene_variant | 0.67 |
ethA | 4327674 | c.-201C>A | upstream_gene_variant | 0.25 |
ethR | 4327777 | p.Asp77Tyr | missense_variant | 0.25 |
ethR | 4327807 | c.260_261delTA | frameshift_variant | 0.25 |
ethA | 4328112 | c.-639G>T | upstream_gene_variant | 0.17 |
ethA | 4328224 | c.-751C>T | upstream_gene_variant | 0.25 |
whiB6 | 4338295 | p.Trp76Leu | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338661 | c.-140C>A | upstream_gene_variant | 0.17 |
whiB6 | 4338698 | c.-177C>A | upstream_gene_variant | 0.15 |
gid | 4407698 | p.Asp169Tyr | missense_variant | 0.33 |
gid | 4407731 | c.472C>A | synonymous_variant | 0.33 |
gid | 4407926 | p.Pro93Thr | missense_variant | 0.25 |
gid | 4408304 | c.-102G>A | upstream_gene_variant | 0.15 |