Run ID: ERR4821486
Sample name:
Date: 01-04-2023 17:16:45
Number of reads: 382118
Percentage reads mapped: 99.29
Strain: lineage2.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
tlyA | 1918211 | p.Ala91Glu | missense_variant | 0.25 | capreomycin |
embB | 4248488 | p.Ala659Thr | missense_variant | 0.18 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5114 | c.-126C>A | upstream_gene_variant | 0.22 |
gyrB | 5287 | c.48T>C | synonymous_variant | 0.25 |
gyrB | 5611 | c.372C>A | synonymous_variant | 0.18 |
gyrB | 5731 | c.492C>T | synonymous_variant | 0.33 |
gyrB | 6263 | p.Asp342His | missense_variant | 0.22 |
gyrB | 6664 | p.Phe475Leu | missense_variant | 0.29 |
gyrB | 6790 | p.Phe517Leu | missense_variant | 0.14 |
gyrB | 7087 | p.Met616Ile | missense_variant | 0.14 |
gyrB | 7097 | p.Glu620* | stop_gained | 0.24 |
gyrB | 7251 | p.Arg671Gln | missense_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7368 | p.Glu23* | stop_gained | 0.15 |
gyrA | 7406 | c.105G>T | synonymous_variant | 0.13 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7642 | p.Gly114Val | missense_variant | 0.17 |
gyrA | 7986 | p.Pro229Thr | missense_variant | 0.2 |
gyrA | 8030 | c.729C>A | synonymous_variant | 0.12 |
gyrA | 8527 | p.Arg409Leu | missense_variant | 0.2 |
gyrA | 8632 | p.Ala444Asp | missense_variant | 0.17 |
gyrA | 8931 | p.Val544Leu | missense_variant | 0.2 |
gyrA | 8949 | p.Lys550* | stop_gained | 0.13 |
gyrA | 9036 | p.Ala579Ser | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9801 | p.Asp834Tyr | missense_variant | 0.29 |
fgd1 | 490748 | c.-35G>T | upstream_gene_variant | 0.29 |
fgd1 | 491289 | c.507C>A | synonymous_variant | 0.33 |
fgd1 | 491308 | p.Ala176Thr | missense_variant | 0.5 |
fgd1 | 491603 | p.Ala274Glu | missense_variant | 0.33 |
fgd1 | 491638 | p.Val286Leu | missense_variant | 0.25 |
fgd1 | 491733 | c.951G>A | synonymous_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575477 | p.Pro44Thr | missense_variant | 0.15 |
mshA | 575769 | p.Ala141Glu | missense_variant | 0.13 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 575990 | p.Val215Phe | missense_variant | 0.14 |
mshA | 576082 | p.Asp245Glu | missense_variant | 0.2 |
mshA | 576505 | c.1158C>T | synonymous_variant | 1.0 |
ccsA | 619717 | c.-174G>T | upstream_gene_variant | 0.4 |
ccsA | 620251 | p.Gly121Trp | missense_variant | 0.15 |
ccsA | 620319 | c.429C>A | synonymous_variant | 0.17 |
ccsA | 620356 | p.Leu156Val | missense_variant | 0.2 |
ccsA | 620503 | p.Glu205* | stop_gained | 0.25 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620629 | p.Gly247Cys | missense_variant | 0.17 |
rpoB | 760064 | p.Glu86Asp | missense_variant | 0.17 |
rpoB | 760426 | p.Glu207Ala | missense_variant | 0.4 |
rpoB | 761168 | c.1362C>A | synonymous_variant | 0.25 |
rpoB | 761258 | p.Glu484Asp | missense_variant | 0.18 |
rpoB | 761260 | p.Gly485Val | missense_variant | 0.18 |
rpoB | 761499 | p.Val565Leu | missense_variant | 0.2 |
rpoB | 761604 | p.Leu600Ile | missense_variant | 0.25 |
rpoB | 761881 | p.Ala692Asp | missense_variant | 0.14 |
rpoB | 761941 | p.Asn712Ser | missense_variant | 0.15 |
rpoB | 762148 | p.Arg781Leu | missense_variant | 0.25 |
rpoB | 762795 | p.Asp997Tyr | missense_variant | 0.25 |
rpoB | 762930 | p.Pro1042Thr | missense_variant | 0.22 |
rpoB | 762992 | c.3190delG | frameshift_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763223 | c.-147C>A | upstream_gene_variant | 0.15 |
rpoC | 763707 | p.Arg113Leu | missense_variant | 0.14 |
rpoC | 763804 | p.His145Gln | missense_variant | 0.14 |
rpoC | 763845 | p.Arg159His | missense_variant | 0.2 |
rpoC | 765052 | c.1683C>G | synonymous_variant | 0.12 |
rpoC | 765179 | p.Gly604Trp | missense_variant | 0.15 |
rpoC | 765400 | c.2031G>T | synonymous_variant | 0.17 |
rpoC | 765835 | c.2466C>G | synonymous_variant | 0.33 |
rpoC | 766211 | p.Glu948* | stop_gained | 0.14 |
rpoC | 766228 | p.Leu953Phe | missense_variant | 0.12 |
rpoC | 766696 | p.Gln1109His | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776471 | p.Gln670His | missense_variant | 0.14 |
mmpL5 | 776922 | p.Ala520Asp | missense_variant | 0.15 |
mmpL5 | 777125 | p.Ser452Arg | missense_variant | 0.17 |
mmpL5 | 777945 | p.Pro179Arg | missense_variant | 0.14 |
mmpL5 | 778119 | p.Thr121Asn | missense_variant | 0.12 |
mmpS5 | 778653 | p.Ala85Ser | missense_variant | 0.18 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781383 | c.-177G>T | upstream_gene_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781700 | c.141G>T | synonymous_variant | 0.17 |
fbiC | 1302870 | c.-61G>T | upstream_gene_variant | 0.17 |
fbiC | 1303042 | p.Thr38Ala | missense_variant | 0.29 |
fbiC | 1303206 | c.276C>T | synonymous_variant | 0.17 |
fbiC | 1303328 | p.Arg133Leu | missense_variant | 0.18 |
fbiC | 1303417 | p.Gly163Cys | missense_variant | 0.15 |
fbiC | 1303546 | p.Pro206Thr | missense_variant | 0.2 |
fbiC | 1303932 | c.1002G>T | synonymous_variant | 0.29 |
Rv1258c | 1406456 | c.885T>C | synonymous_variant | 0.2 |
Rv1258c | 1406603 | c.738G>A | synonymous_variant | 0.15 |
Rv1258c | 1406621 | c.720G>T | synonymous_variant | 0.17 |
Rv1258c | 1406697 | p.Gly215Ala | missense_variant | 0.2 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407264 | p.Ser26* | stop_gained | 0.67 |
Rv1258c | 1407282 | p.Ala20Asp | missense_variant | 0.25 |
embR | 1416502 | p.Met282Ile | missense_variant | 0.2 |
embR | 1416695 | p.Ser218Tyr | missense_variant | 0.14 |
embR | 1416988 | c.360C>G | synonymous_variant | 0.5 |
embR | 1417284 | p.Thr22Ser | missense_variant | 0.12 |
atpE | 1461233 | c.189A>G | synonymous_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471761 | n.-85G>T | upstream_gene_variant | 0.19 |
rrs | 1472063 | n.218C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472562 | n.717C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472577 | n.732G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472633 | n.788C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472768 | n.923C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473166 | n.1321G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473427 | n.-231G>T | upstream_gene_variant | 0.2 |
rrl | 1473548 | n.-109delG | upstream_gene_variant | 0.14 |
rrl | 1474372 | n.715C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474661 | n.1004G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474857 | n.1200G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475520 | n.1863G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475993 | n.2336C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476744 | n.3087G>T | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1673195 | c.-245C>G | upstream_gene_variant | 0.22 |
fabG1 | 1673329 | c.-111A>G | upstream_gene_variant | 0.11 |
fabG1 | 1673699 | p.Ser87Tyr | missense_variant | 0.2 |
fabG1 | 1674118 | p.Glu227* | stop_gained | 0.5 |
inhA | 1674295 | p.Gln32Lys | missense_variant | 0.22 |
rpsA | 1833426 | c.-116T>A | upstream_gene_variant | 0.5 |
rpsA | 1833599 | p.Glu20* | stop_gained | 0.15 |
rpsA | 1833628 | c.87G>A | synonymous_variant | 0.15 |
rpsA | 1833745 | c.204G>T | synonymous_variant | 0.13 |
rpsA | 1833903 | p.Glu121Gly | missense_variant | 0.67 |
rpsA | 1833933 | p.Ile131Thr | missense_variant | 0.29 |
rpsA | 1833972 | p.Leu144Pro | missense_variant | 0.2 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834239 | p.Gly233Val | missense_variant | 0.18 |
rpsA | 1834324 | p.Glu261Asp | missense_variant | 0.17 |
rpsA | 1834328 | p.Leu263Ile | missense_variant | 0.17 |
rpsA | 1834353 | p.Arg271Leu | missense_variant | 0.17 |
rpsA | 1834373 | p.Ala278Ser | missense_variant | 0.17 |
rpsA | 1834429 | c.888C>T | synonymous_variant | 0.29 |
rpsA | 1834484 | p.Glu315* | stop_gained | 0.5 |
rpsA | 1834754 | p.Glu405* | stop_gained | 0.15 |
tlyA | 1917858 | c.-82G>T | upstream_gene_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918365 | p.Glu142Asp | missense_variant | 0.33 |
tlyA | 1918741 | p.Pro268Ala | missense_variant | 0.2 |
ndh | 2101878 | p.Gly389Arg | missense_variant | 0.12 |
ndh | 2102079 | p.Asp322Asn | missense_variant | 0.22 |
katG | 2154206 | p.Ala636Thr | missense_variant | 0.17 |
katG | 2154207 | c.1905C>A | synonymous_variant | 0.17 |
katG | 2154329 | p.Arg595* | stop_gained | 0.33 |
katG | 2154608 | p.Gln502Lys | missense_variant | 0.15 |
katG | 2154617 | p.Leu499Met | missense_variant | 0.18 |
katG | 2154636 | c.1476C>G | synonymous_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154775 | p.Ser446Ile | missense_variant | 1.0 |
katG | 2155958 | p.Pro52Thr | missense_variant | 0.18 |
katG | 2156065 | p.Ala16Asp | missense_variant | 0.13 |
katG | 2156097 | p.His5Gln | missense_variant | 0.12 |
katG | 2156153 | c.-42C>T | upstream_gene_variant | 0.13 |
katG | 2156211 | c.-100G>T | upstream_gene_variant | 0.12 |
katG | 2156245 | c.-134G>A | upstream_gene_variant | 0.18 |
PPE35 | 2167692 | p.Gly974Asp | missense_variant | 0.14 |
PPE35 | 2167877 | p.Ser912Arg | missense_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168041 | p.Ala858Thr | missense_variant | 0.33 |
PPE35 | 2168270 | c.2343G>T | synonymous_variant | 0.12 |
PPE35 | 2169023 | c.1590G>T | synonymous_variant | 0.17 |
PPE35 | 2169542 | c.1071C>A | synonymous_variant | 0.13 |
PPE35 | 2169651 | p.Leu321Ser | missense_variant | 0.13 |
PPE35 | 2169794 | c.819C>A | synonymous_variant | 0.18 |
Rv1979c | 2221809 | c.1356C>T | synonymous_variant | 0.2 |
Rv1979c | 2221843 | p.Arg441Leu | missense_variant | 0.25 |
Rv1979c | 2221881 | c.1284G>A | synonymous_variant | 0.17 |
Rv1979c | 2222189 | p.Leu326Ile | missense_variant | 0.13 |
Rv1979c | 2222286 | c.879G>T | synonymous_variant | 0.25 |
Rv1979c | 2222404 | p.Arg254Ile | missense_variant | 0.13 |
Rv1979c | 2222441 | p.Ala242Ser | missense_variant | 0.17 |
Rv1979c | 2222603 | p.Gln188Lys | missense_variant | 0.17 |
Rv1979c | 2222789 | p.Ala126Ser | missense_variant | 0.13 |
Rv1979c | 2222847 | p.Trp106Cys | missense_variant | 0.13 |
Rv1979c | 2222991 | c.174G>T | synonymous_variant | 0.25 |
Rv1979c | 2223110 | p.Val19Ile | missense_variant | 0.15 |
Rv1979c | 2223266 | c.-102G>C | upstream_gene_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223324 | c.-160G>T | upstream_gene_variant | 0.18 |
pncA | 2289621 | c.-380C>A | upstream_gene_variant | 0.22 |
pncA | 2290233 | c.-992C>A | upstream_gene_variant | 0.29 |
kasA | 2518094 | c.-21G>T | upstream_gene_variant | 0.17 |
kasA | 2518347 | p.Arg78Gln | missense_variant | 0.29 |
kasA | 2518621 | c.507G>T | synonymous_variant | 0.18 |
kasA | 2518769 | p.Arg219Ser | missense_variant | 0.67 |
eis | 2714139 | c.1194C>A | synonymous_variant | 0.18 |
eis | 2714663 | p.Ala224Ser | missense_variant | 0.29 |
eis | 2714710 | p.Pro208His | missense_variant | 0.4 |
eis | 2714814 | c.519C>A | synonymous_variant | 0.5 |
eis | 2714834 | p.Arg167Gly | missense_variant | 0.5 |
eis | 2715324 | c.9G>T | synonymous_variant | 0.18 |
ahpC | 2725921 | c.-272A>T | upstream_gene_variant | 1.0 |
ahpC | 2726054 | c.-139C>A | upstream_gene_variant | 0.15 |
ahpC | 2726294 | c.102C>T | synonymous_variant | 0.15 |
folC | 2746807 | c.792G>A | synonymous_variant | 0.13 |
folC | 2746831 | c.768G>T | synonymous_variant | 0.13 |
folC | 2746896 | p.Gly235Trp | missense_variant | 0.29 |
folC | 2746948 | c.651G>T | synonymous_variant | 0.25 |
folC | 2747142 | p.Glu153* | stop_gained | 0.22 |
pepQ | 2859350 | p.Gln357Lys | missense_variant | 0.25 |
pepQ | 2859355 | p.Ala355Asp | missense_variant | 0.18 |
pepQ | 2859753 | p.Phe222Leu | missense_variant | 0.25 |
pepQ | 2859910 | p.Arg170Leu | missense_variant | 0.33 |
pepQ | 2860254 | c.165C>A | synonymous_variant | 0.29 |
ribD | 2986783 | c.-56C>A | upstream_gene_variant | 0.2 |
ribD | 2987096 | c.258C>A | synonymous_variant | 0.29 |
ribD | 2987256 | p.Pro140Thr | missense_variant | 0.33 |
ribD | 2987541 | p.Leu235Met | missense_variant | 0.4 |
Rv2752c | 3064778 | p.Phe472Leu | missense_variant | 0.2 |
Rv2752c | 3065163 | c.1029C>A | synonymous_variant | 0.2 |
Rv2752c | 3065361 | c.831C>A | synonymous_variant | 0.17 |
Rv2752c | 3065705 | p.Gly163* | stop_gained | 0.22 |
Rv2752c | 3066134 | p.Ala20Thr | missense_variant | 0.14 |
Rv2752c | 3066357 | c.-166G>A | upstream_gene_variant | 0.22 |
thyX | 3067413 | p.Ala178Asp | missense_variant | 0.29 |
thyX | 3067505 | c.441G>T | synonymous_variant | 0.18 |
thyA | 3073803 | p.Glu223Asp | missense_variant | 0.29 |
thyA | 3074234 | p.Trp80Arg | missense_variant | 0.18 |
thyA | 3074555 | c.-84C>A | upstream_gene_variant | 0.15 |
thyA | 3074566 | c.-95G>T | upstream_gene_variant | 0.15 |
ald | 3086684 | c.-136G>T | upstream_gene_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086981 | c.162C>A | synonymous_variant | 0.25 |
ald | 3087020 | p.Asp67Glu | missense_variant | 0.18 |
ald | 3087198 | p.Leu127Ile | missense_variant | 0.14 |
ald | 3087794 | c.975C>T | synonymous_variant | 0.25 |
ald | 3087821 | c.1002G>T | synonymous_variant | 0.2 |
fbiD | 3339087 | c.-31C>A | upstream_gene_variant | 0.18 |
fbiD | 3339306 | c.189C>A | synonymous_variant | 0.4 |
fbiD | 3339372 | c.255C>A | synonymous_variant | 0.5 |
fbiD | 3339728 | p.Gly204Val | missense_variant | 0.15 |
Rv3083 | 3448389 | c.-115C>A | upstream_gene_variant | 0.29 |
Rv3083 | 3449010 | p.Trp169* | stop_gained | 0.14 |
Rv3083 | 3449147 | p.Ser215* | stop_gained | 0.5 |
Rv3083 | 3449193 | c.690G>T | synonymous_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474453 | c.447G>A | synonymous_variant | 0.13 |
fprA | 3474455 | p.Ala150Asp | missense_variant | 0.13 |
fprA | 3475311 | p.Glu435Asp | missense_variant | 0.33 |
whiB7 | 3568576 | p.Gly35Val | missense_variant | 0.18 |
Rv3236c | 3612060 | p.Ala353Thr | missense_variant | 0.14 |
Rv3236c | 3612518 | p.Tyr200Cys | missense_variant | 0.4 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3612838 | c.279G>T | synonymous_variant | 0.33 |
Rv3236c | 3612978 | p.Gly47Ser | missense_variant | 0.25 |
Rv3236c | 3613001 | p.Ala39Gly | missense_variant | 0.14 |
Rv3236c | 3613165 | c.-49G>T | upstream_gene_variant | 0.14 |
fbiA | 3640618 | p.Gly26Ser | missense_variant | 0.22 |
fbiA | 3640627 | p.Ala29Ser | missense_variant | 0.22 |
fbiA | 3640907 | p.Gly122Val | missense_variant | 0.22 |
fbiB | 3642036 | p.Ala168Ser | missense_variant | 0.33 |
fbiB | 3642309 | p.Leu259Met | missense_variant | 0.25 |
fbiB | 3642350 | c.816G>T | synonymous_variant | 0.22 |
fbiB | 3642380 | p.Glu282Asp | missense_variant | 0.17 |
fbiB | 3642847 | p.Pro438Gln | missense_variant | 0.5 |
alr | 3840459 | p.Ser321* | stop_gained | 0.2 |
alr | 3840671 | c.750G>A | synonymous_variant | 0.22 |
alr | 3840894 | p.Leu176Gln | missense_variant | 0.25 |
alr | 3841014 | p.Arg136Pro | missense_variant | 0.22 |
alr | 3841030 | p.Ala131Ser | missense_variant | 0.18 |
alr | 3841507 | c.-87C>T | upstream_gene_variant | 0.13 |
alr | 3841515 | c.-95C>A | upstream_gene_variant | 0.13 |
rpoA | 3877722 | p.Asn262Lys | missense_variant | 0.33 |
rpoA | 3877760 | p.Pro250Thr | missense_variant | 0.2 |
rpoA | 3877811 | p.Glu233* | stop_gained | 0.22 |
rpoA | 3877899 | p.Ser203Arg | missense_variant | 0.17 |
rpoA | 3878319 | p.Phe63Leu | missense_variant | 0.15 |
rpoA | 3878503 | p.Leu2Gln | missense_variant | 0.4 |
ddn | 3986742 | c.-102G>A | upstream_gene_variant | 0.25 |
ddn | 3986749 | c.-95C>A | upstream_gene_variant | 0.22 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.14 |
clpC1 | 4038750 | p.Gly652Val | missense_variant | 0.5 |
clpC1 | 4039208 | c.1497C>A | synonymous_variant | 0.29 |
clpC1 | 4039325 | p.Gln460His | missense_variant | 0.15 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.12 |
clpC1 | 4040314 | p.Leu131Met | missense_variant | 0.29 |
clpC1 | 4040375 | c.330G>T | synonymous_variant | 0.17 |
clpC1 | 4040894 | c.-190G>T | upstream_gene_variant | 0.25 |
panD | 4043967 | c.315C>A | synonymous_variant | 0.4 |
embC | 4240585 | c.723C>A | synonymous_variant | 0.29 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.29 |
embC | 4241507 | p.Ala549Thr | missense_variant | 0.13 |
embC | 4241706 | p.Ser615Leu | missense_variant | 0.22 |
embC | 4242090 | p.Ala743Val | missense_variant | 0.29 |
embC | 4242629 | p.Ala923Ser | missense_variant | 0.22 |
embC | 4242641 | p.Arg927Ser | missense_variant | 0.22 |
embC | 4242771 | p.Thr970Lys | missense_variant | 0.4 |
embA | 4242856 | c.-377C>A | upstream_gene_variant | 0.33 |
embA | 4243315 | p.Cys28Phe | missense_variant | 0.2 |
embA | 4243318 | p.Gly29Val | missense_variant | 0.2 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244813 | p.Cys527* | stop_gained | 0.14 |
embA | 4244877 | p.Ala549Ser | missense_variant | 0.29 |
embA | 4244904 | p.Val558Leu | missense_variant | 1.0 |
embA | 4244918 | c.1686G>T | synonymous_variant | 0.17 |
embA | 4245404 | c.2172C>G | synonymous_variant | 0.18 |
embB | 4245545 | c.-969C>T | upstream_gene_variant | 0.29 |
embA | 4245569 | p.Glu779Asp | missense_variant | 0.22 |
embA | 4245682 | p.Gly817Val | missense_variant | 0.29 |
embB | 4246331 | c.-183C>G | upstream_gene_variant | 0.4 |
embB | 4247344 | c.831C>T | synonymous_variant | 0.18 |
embB | 4247425 | c.912G>A | synonymous_variant | 0.17 |
embB | 4247435 | p.Arg308* | stop_gained | 0.25 |
embB | 4247779 | c.1266C>A | synonymous_variant | 0.22 |
embB | 4247969 | p.Gly486Arg | missense_variant | 0.67 |
embB | 4248171 | p.Ala553Glu | missense_variant | 0.25 |
embB | 4248204 | p.Pro564Arg | missense_variant | 0.25 |
embB | 4248280 | c.1767C>A | synonymous_variant | 0.12 |
embB | 4248292 | c.1779G>T | synonymous_variant | 0.14 |
embB | 4248840 | p.Pro776His | missense_variant | 0.17 |
embB | 4248915 | p.Ala801Glu | missense_variant | 0.33 |
embB | 4249687 | c.3174C>A | synonymous_variant | 0.17 |
embB | 4249754 | p.Gly1081Cys | missense_variant | 0.17 |
aftB | 4267329 | p.Arg503Leu | missense_variant | 0.4 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267814 | c.1023G>T | synonymous_variant | 0.22 |
aftB | 4267827 | p.Arg337Pro | missense_variant | 0.29 |
aftB | 4268033 | c.804G>T | synonymous_variant | 0.12 |
aftB | 4268186 | c.651C>A | synonymous_variant | 0.22 |
aftB | 4268402 | p.Leu145Phe | missense_variant | 0.15 |
ubiA | 4269417 | p.Cys139* | stop_gained | 0.25 |
aftB | 4269492 | c.-656G>T | upstream_gene_variant | 0.25 |
ubiA | 4269866 | c.-33G>C | upstream_gene_variant | 0.33 |
ubiA | 4269891 | c.-58G>T | upstream_gene_variant | 0.33 |
ethA | 4326020 | p.Ala485Asp | missense_variant | 0.2 |
ethA | 4326305 | p.Ser390Tyr | missense_variant | 0.2 |
ethA | 4326380 | p.Thr365Lys | missense_variant | 0.33 |
ethA | 4326735 | p.Ala247Ser | missense_variant | 0.13 |
ethR | 4326997 | c.-552C>A | upstream_gene_variant | 0.33 |
ethR | 4327084 | c.-465G>A | upstream_gene_variant | 1.0 |
ethA | 4327216 | p.Lys86Asn | missense_variant | 0.25 |
ethA | 4327262 | p.Gly71Ala | missense_variant | 0.33 |
ethA | 4327421 | p.Ser18Ile | missense_variant | 0.14 |
ethR | 4328193 | p.Asn215Lys | missense_variant | 0.33 |
ethA | 4328212 | c.-739G>T | upstream_gene_variant | 0.29 |
ethA | 4328262 | c.-789C>A | upstream_gene_variant | 0.18 |
whiB6 | 4338182 | p.Gln114Lys | missense_variant | 0.18 |
whiB6 | 4338277 | p.Pro82His | missense_variant | 0.33 |
whiB6 | 4338284 | p.Val80Ile | missense_variant | 0.33 |
whiB6 | 4338437 | p.Val29Phe | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338712 | c.-191T>C | upstream_gene_variant | 0.12 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4407975 | c.228C>A | synonymous_variant | 0.15 |
gid | 4408143 | c.60G>T | synonymous_variant | 0.14 |