Run ID: ERR3797024
Sample name:
Date: 01-04-2023 03:02:34
Number of reads: 30303
Percentage reads mapped: 18.58
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6634 | c.-668T>C | upstream_gene_variant | 0.67 |
gyrA | 6637 | c.-665T>G | upstream_gene_variant | 0.67 |
gyrA | 6640 | c.-662A>C | upstream_gene_variant | 0.67 |
gyrA | 6643 | c.-659A>G | upstream_gene_variant | 0.67 |
gyrA | 6649 | c.-653T>C | upstream_gene_variant | 0.67 |
gyrA | 6655 | c.-647T>C | upstream_gene_variant | 0.67 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.67 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7442 | c.141G>T | synonymous_variant | 0.5 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.75 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.75 |
gyrA | 7463 | c.162G>C | synonymous_variant | 0.5 |
gyrA | 7469 | c.168C>G | synonymous_variant | 0.5 |
gyrA | 7472 | c.171T>C | synonymous_variant | 0.75 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.67 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.75 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.75 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.67 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.67 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.67 |
gyrA | 8438 | c.1137C>T | synonymous_variant | 1.0 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 1.0 |
gyrA | 8459 | c.1158G>A | synonymous_variant | 1.0 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 1.0 |
gyrA | 8468 | c.1167C>T | synonymous_variant | 1.0 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 1.0 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 1.0 |
gyrA | 8510 | c.1209G>A | synonymous_variant | 1.0 |
gyrA | 8561 | c.1260A>G | synonymous_variant | 1.0 |
gyrA | 8573 | c.1272G>C | synonymous_variant | 1.0 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 1.0 |
gyrA | 9029 | c.1728T>G | synonymous_variant | 1.0 |
gyrA | 9050 | p.Asp583Glu | missense_variant | 1.0 |
gyrA | 9051 | c.1750T>C | synonymous_variant | 1.0 |
gyrA | 9056 | c.1755C>G | synonymous_variant | 1.0 |
gyrA | 9062 | c.1761C>T | synonymous_variant | 1.0 |
gyrA | 9071 | c.1770G>C | synonymous_variant | 1.0 |
gyrA | 9074 | c.1773G>C | synonymous_variant | 1.0 |
gyrA | 9080 | c.1779G>T | synonymous_variant | 1.0 |
gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 1.0 |
gyrA | 9104 | c.1803C>T | synonymous_variant | 1.0 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 1.0 |
gyrA | 9131 | c.1830G>A | synonymous_variant | 1.0 |
gyrA | 9134 | c.1833C>G | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9153 | p.Thr618Ala | missense_variant | 1.0 |
fgd1 | 490887 | c.105G>C | synonymous_variant | 1.0 |
fgd1 | 490902 | c.120T>C | synonymous_variant | 1.0 |
fgd1 | 490905 | c.123T>C | synonymous_variant | 1.0 |
fgd1 | 490911 | c.129T>G | synonymous_variant | 1.0 |
fgd1 | 490921 | p.Gln47Glu | missense_variant | 0.67 |
fgd1 | 491191 | p.Gly137Arg | missense_variant | 1.0 |
fgd1 | 491196 | c.414A>G | synonymous_variant | 1.0 |
fgd1 | 491244 | c.462T>C | synonymous_variant | 0.5 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 0.5 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 0.5 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 0.5 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 0.5 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.5 |
fgd1 | 491331 | c.549G>A | synonymous_variant | 0.67 |
mshA | 575629 | c.282A>G | synonymous_variant | 0.5 |
mshA | 575632 | c.285G>C | synonymous_variant | 0.5 |
mshA | 575635 | c.288A>C | synonymous_variant | 0.5 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.5 |
mshA | 575647 | c.300G>C | synonymous_variant | 0.5 |
mshA | 575649 | p.Val101Glu | missense_variant | 0.5 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.5 |
ccsA | 620295 | c.405G>T | synonymous_variant | 0.67 |
ccsA | 620307 | c.417C>A | synonymous_variant | 0.67 |
ccsA | 620319 | c.429C>G | synonymous_variant | 0.67 |
ccsA | 620367 | c.477T>C | synonymous_variant | 1.0 |
ccsA | 620373 | c.483C>G | synonymous_variant | 1.0 |
ccsA | 620385 | c.495G>C | synonymous_variant | 1.0 |
ccsA | 620388 | c.498A>G | synonymous_variant | 1.0 |
ccsA | 620409 | c.519C>G | synonymous_variant | 1.0 |
ccsA | 620415 | c.525T>C | synonymous_variant | 1.0 |
ccsA | 620433 | c.543C>G | synonymous_variant | 1.0 |
ccsA | 620436 | c.546T>C | synonymous_variant | 1.0 |
ccsA | 620439 | c.549T>G | synonymous_variant | 1.0 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.67 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.67 |
rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
rpoB | 760481 | c.675G>C | synonymous_variant | 1.0 |
rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
rpoB | 760514 | c.708C>T | synonymous_variant | 1.0 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.67 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.67 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.67 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.67 |
rpoB | 760856 | c.1050C>G | synonymous_variant | 1.0 |
rpoB | 760862 | c.1056G>C | synonymous_variant | 1.0 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 1.0 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 1.0 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 1.0 |
rpoB | 760934 | c.1128C>G | synonymous_variant | 1.0 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 1.0 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 1.0 |
rpoB | 761180 | c.1374A>G | synonymous_variant | 0.67 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.67 |
rpoB | 761196 | c.1390C>T | synonymous_variant | 0.67 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.67 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.67 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.67 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.67 |
rpoB | 762119 | c.2313C>T | synonymous_variant | 0.67 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.67 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.67 |
rpoB | 762149 | c.2343G>T | synonymous_variant | 0.67 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 1.0 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.83 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.67 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.67 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.67 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
rpoB | 762297 | c.2491C>T | synonymous_variant | 0.75 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 1.0 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 1.0 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 1.0 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 1.0 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 1.0 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 1.0 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 1.0 |
rpoB | 762490 | p.Val895Ala | missense_variant | 1.0 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 1.0 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 1.0 |
rpoC | 762521 | c.-849C>G | upstream_gene_variant | 0.8 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.75 |
rpoC | 762536 | c.-834T>C | upstream_gene_variant | 0.75 |
rpoC | 762537 | c.-833T>C | upstream_gene_variant | 0.75 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.75 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.4 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.4 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.4 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.4 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.4 |
rpoC | 763052 | c.-318G>C | upstream_gene_variant | 0.4 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.4 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.4 |
rpoC | 763082 | c.-288C>G | upstream_gene_variant | 0.4 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.5 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.5 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.75 |
rpoC | 763486 | c.117T>G | synonymous_variant | 1.0 |
rpoC | 763528 | c.159G>A | synonymous_variant | 1.0 |
rpoC | 763537 | c.168C>G | synonymous_variant | 1.0 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
rpoC | 763573 | c.204G>C | synonymous_variant | 1.0 |
rpoC | 763594 | c.225C>T | synonymous_variant | 1.0 |
rpoC | 763600 | c.231C>G | synonymous_variant | 1.0 |
rpoC | 763858 | c.489A>G | synonymous_variant | 1.0 |
rpoC | 763871 | p.Gly168Thr | missense_variant | 1.0 |
rpoC | 763879 | c.510A>G | synonymous_variant | 1.0 |
rpoC | 763888 | c.519G>T | synonymous_variant | 1.0 |
rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
rpoC | 765292 | c.1923G>T | synonymous_variant | 1.0 |
rpoC | 765300 | p.Val644Ala | missense_variant | 1.0 |
rpoC | 765327 | p.His653Pro | missense_variant | 1.0 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 1.0 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 1.0 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 1.0 |
rpoC | 766531 | c.3162G>T | synonymous_variant | 1.0 |
rpoC | 766540 | p.Asp1057Glu | missense_variant | 1.0 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 1.0 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 1.0 |
rpoC | 766582 | c.3213C>G | synonymous_variant | 1.0 |
rpoC | 766585 | c.3216T>C | synonymous_variant | 1.0 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 1.0 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 1.0 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 1.0 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 1.0 |
rpoC | 766627 | c.3258G>C | synonymous_variant | 1.0 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 1.0 |
rpoC | 767032 | c.3663G>C | synonymous_variant | 1.0 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
rpoC | 767062 | c.3693C>G | synonymous_variant | 1.0 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 1.0 |
rpsL | 781608 | p.Ser17Gly | missense_variant | 1.0 |
rpsL | 781628 | c.69T>C | synonymous_variant | 1.0 |
rpsL | 781649 | c.90T>C | synonymous_variant | 1.0 |
rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
rpsL | 781682 | c.123T>G | synonymous_variant | 1.0 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.8 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.8 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.75 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.67 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.67 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.67 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.67 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.67 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.67 |
rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
rpsL | 781877 | c.318T>C | synonymous_variant | 1.0 |
rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.67 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.67 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 1.0 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
rplC | 800814 | c.6A>G | synonymous_variant | 1.0 |
rplC | 800844 | c.36T>C | synonymous_variant | 1.0 |
fbiC | 1303674 | c.744C>G | synonymous_variant | 0.5 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.5 |
fbiC | 1303731 | c.801A>G | synonymous_variant | 0.5 |
fbiC | 1303732 | p.Ser268Pro | missense_variant | 0.5 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.5 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 0.4 |
fbiC | 1303749 | c.819G>C | synonymous_variant | 0.5 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 0.5 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 0.5 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 0.67 |
fbiC | 1303794 | c.864A>G | synonymous_variant | 0.67 |
fbiC | 1303806 | c.876G>A | synonymous_variant | 0.67 |
fbiC | 1303809 | c.879G>A | synonymous_variant | 0.67 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.5 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.67 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.67 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.67 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.67 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.67 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472085 | n.240C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472086 | n.241T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472089 | n.244C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472282 | n.437T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472498 | n.653C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472518 | n.673G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472544 | n.699C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472659 | n.814G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472678 | n.834_840delTCCTTGG | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472687 | n.842_843insCC | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472698 | n.853A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474950 | n.1293G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474952 | n.1296_1300delCATCC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474961 | n.1304T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474962 | n.1305T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474963 | n.1306G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474964 | n.1307T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474967 | n.1311_1315delGGGTG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474997 | n.1340A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475006 | n.1349A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475253 | n.1596T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475273 | n.1616T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475289 | n.1632G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475366 | n.1709G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476238 | n.2581T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476248 | n.2591G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476252 | n.2595T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476259 | n.2602C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476298 | n.2642_2644delCGA | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476306 | n.2649A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476573 | n.2916A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476608 | n.2951C>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674542 | p.Ala114Glu | missense_variant | 1.0 |
inhA | 1674546 | c.345T>C | synonymous_variant | 1.0 |
inhA | 1674549 | c.348G>C | synonymous_variant | 1.0 |
inhA | 1674550 | p.Ser117Ala | missense_variant | 1.0 |
inhA | 1674570 | c.369G>C | synonymous_variant | 1.0 |
inhA | 1674576 | c.375T>C | synonymous_variant | 1.0 |
inhA | 1674582 | c.381T>C | synonymous_variant | 1.0 |
inhA | 1674585 | c.384T>C | synonymous_variant | 1.0 |
inhA | 1674589 | p.Met130Leu | missense_variant | 1.0 |
inhA | 1674624 | c.423A>C | synonymous_variant | 1.0 |
inhA | 1674627 | c.426T>C | synonymous_variant | 1.0 |
inhA | 1674628 | p.Ser143Gly | missense_variant | 1.0 |
inhA | 1674654 | c.453G>C | synonymous_variant | 1.0 |
inhA | 1674660 | c.459G>T | synonymous_variant | 1.0 |
inhA | 1674663 | c.462G>C | synonymous_variant | 1.0 |
inhA | 1674703 | c.502T>C | synonymous_variant | 1.0 |
inhA | 1674714 | c.513C>G | synonymous_variant | 1.0 |
inhA | 1674718 | c.517A>C | synonymous_variant | 1.0 |
inhA | 1674726 | c.525G>A | synonymous_variant | 1.0 |
inhA | 1674729 | c.528G>C | synonymous_variant | 1.0 |
inhA | 1674750 | c.549T>C | synonymous_variant | 1.0 |
inhA | 1674756 | c.555T>C | synonymous_variant | 1.0 |
inhA | 1674765 | c.564C>T | synonymous_variant | 1.0 |
inhA | 1674771 | c.570C>G | synonymous_variant | 1.0 |
inhA | 1674777 | c.576C>G | synonymous_variant | 1.0 |
inhA | 1674780 | c.579T>G | synonymous_variant | 1.0 |
inhA | 1674792 | c.591G>C | synonymous_variant | 1.0 |
inhA | 1674801 | c.600T>C | synonymous_variant | 1.0 |
inhA | 1674816 | c.615T>A | synonymous_variant | 1.0 |
inhA | 1674822 | c.621C>G | synonymous_variant | 1.0 |
inhA | 1674825 | c.624C>T | synonymous_variant | 1.0 |
inhA | 1674846 | c.645C>A | synonymous_variant | 1.0 |
inhA | 1674957 | c.756G>A | synonymous_variant | 1.0 |
inhA | 1674966 | c.765T>C | synonymous_variant | 1.0 |
inhA | 1674967 | p.Asp256Thr | missense_variant | 1.0 |
inhA | 1674970 | p.Ile257Val | missense_variant | 1.0 |
rpsA | 1833673 | c.132C>A | synonymous_variant | 0.67 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 1.0 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 1.0 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.75 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 1.0 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
ndh | 2101838 | p.Ala402Val | missense_variant | 0.5 |
ndh | 2101858 | p.Ile395Met | missense_variant | 0.5 |
ndh | 2101873 | c.1170T>C | synonymous_variant | 0.5 |
ndh | 2101888 | p.Val385Leu | missense_variant | 0.5 |
ndh | 2101891 | c.1152C>G | synonymous_variant | 0.5 |
ndh | 2101912 | c.1131G>C | synonymous_variant | 0.5 |
ndh | 2101920 | c.1123A>C | synonymous_variant | 0.75 |
ndh | 2101924 | c.1119T>G | synonymous_variant | 0.75 |
ndh | 2101936 | c.1107G>C | synonymous_variant | 0.75 |
ndh | 2101939 | c.1104A>G | synonymous_variant | 0.75 |
ndh | 2101960 | c.1083A>C | synonymous_variant | 0.75 |
ndh | 2102269 | c.774C>G | synonymous_variant | 1.0 |
ndh | 2102287 | c.756C>G | synonymous_variant | 0.67 |
ndh | 2102311 | c.732G>A | synonymous_variant | 0.67 |
ndh | 2102317 | c.726A>G | synonymous_variant | 0.67 |
ndh | 2102320 | c.723G>C | synonymous_variant | 0.67 |
ndh | 2102341 | c.702C>A | synonymous_variant | 0.67 |
ndh | 2102344 | c.699T>C | synonymous_variant | 0.67 |
ndh | 2102366 | p.Ala226Glu | missense_variant | 0.67 |
ndh | 2102377 | c.666A>G | synonymous_variant | 0.67 |
ndh | 2102382 | c.661C>T | synonymous_variant | 0.67 |
ndh | 2102389 | c.654G>C | synonymous_variant | 0.67 |
ndh | 2102392 | c.651C>G | synonymous_variant | 0.67 |
ndh | 2102401 | c.642T>C | synonymous_variant | 0.67 |
ndh | 2102680 | c.363T>C | synonymous_variant | 1.0 |
ndh | 2102683 | c.360T>C | synonymous_variant | 1.0 |
ndh | 2102712 | p.Pro111Ser | missense_variant | 1.0 |
ndh | 2102718 | p.Gln109Glu | missense_variant | 1.0 |
ndh | 2102728 | c.315T>C | synonymous_variant | 1.0 |
ndh | 2102737 | p.Glu102Asp | missense_variant | 1.0 |
ndh | 2102740 | c.303G>C | synonymous_variant | 1.0 |
ndh | 2102743 | c.300C>G | synonymous_variant | 1.0 |
ndh | 2102746 | c.297C>G | synonymous_variant | 1.0 |
ndh | 2102750 | p.Cys98Thr | missense_variant | 1.0 |
ndh | 2102755 | p.Gly96Asn | missense_variant | 1.0 |
ndh | 2102771 | p.His91Gly | missense_variant | 1.0 |
ndh | 2102787 | c.256T>C | synonymous_variant | 1.0 |
ndh | 2102791 | c.252A>G | synonymous_variant | 1.0 |
ndh | 2102830 | c.213G>C | synonymous_variant | 1.0 |
kasA | 2517920 | c.-195G>A | upstream_gene_variant | 1.0 |
kasA | 2518699 | p.Cys195* | stop_gained | 1.0 |
kasA | 2518711 | c.597A>G | synonymous_variant | 1.0 |
kasA | 2518714 | c.600A>C | synonymous_variant | 1.0 |
kasA | 2518717 | c.603C>G | synonymous_variant | 1.0 |
kasA | 2518747 | c.633C>G | synonymous_variant | 1.0 |
kasA | 2518783 | c.669T>C | synonymous_variant | 1.0 |
kasA | 2518789 | c.675G>C | synonymous_variant | 1.0 |
kasA | 2518795 | c.681C>A | synonymous_variant | 1.0 |
kasA | 2518798 | c.684G>T | synonymous_variant | 1.0 |
kasA | 2518825 | c.711T>C | synonymous_variant | 1.0 |
kasA | 2518843 | c.729T>G | synonymous_variant | 0.67 |
kasA | 2518849 | c.735G>C | synonymous_variant | 0.67 |
kasA | 2519152 | c.1038G>C | synonymous_variant | 0.67 |
kasA | 2519167 | c.1053T>C | synonymous_variant | 1.0 |
kasA | 2519173 | c.1059C>G | synonymous_variant | 1.0 |
kasA | 2519176 | c.1062G>A | synonymous_variant | 1.0 |
kasA | 2519179 | c.1065G>T | synonymous_variant | 0.67 |
kasA | 2519182 | c.1068G>C | synonymous_variant | 0.67 |
kasA | 2519191 | c.1077G>A | synonymous_variant | 0.67 |
kasA | 2519192 | c.1078C>T | synonymous_variant | 0.67 |
kasA | 2519197 | c.1083G>C | synonymous_variant | 1.0 |
kasA | 2519200 | c.1086G>T | synonymous_variant | 0.67 |
kasA | 2519203 | c.1089C>G | synonymous_variant | 0.67 |
kasA | 2519215 | c.1101C>A | synonymous_variant | 1.0 |
kasA | 2519221 | c.1107G>C | synonymous_variant | 1.0 |
kasA | 2519224 | c.1110C>G | synonymous_variant | 1.0 |
kasA | 2519239 | c.1125A>C | synonymous_variant | 1.0 |
kasA | 2519263 | c.1149C>T | synonymous_variant | 1.0 |
kasA | 2519266 | c.1152C>T | synonymous_variant | 1.0 |
kasA | 2519272 | c.1158C>G | synonymous_variant | 1.0 |
kasA | 2519281 | c.1167G>T | synonymous_variant | 1.0 |
folC | 2746728 | c.871T>C | synonymous_variant | 1.0 |
folC | 2746734 | p.Ile289Val | missense_variant | 1.0 |
folC | 2746744 | c.855T>G | synonymous_variant | 1.0 |
folC | 2746759 | c.840G>A | synonymous_variant | 1.0 |
folC | 2746765 | c.834A>G | synonymous_variant | 1.0 |
folC | 2746771 | c.828A>C | synonymous_variant | 1.0 |
folC | 2746777 | c.822T>A | synonymous_variant | 1.0 |
folC | 2746785 | p.Val272Ile | missense_variant | 1.0 |
folC | 2746791 | p.Ile270Val | missense_variant | 1.0 |
folC | 2746793 | p.Gln269Arg | missense_variant | 1.0 |
folC | 2746795 | c.804A>C | synonymous_variant | 1.0 |
folC | 2746798 | p.Arg267Gly | missense_variant | 1.0 |
folC | 2746801 | c.796_798delCTAinsTTG | synonymous_variant | 1.0 |
folC | 2746813 | c.786A>G | synonymous_variant | 1.0 |
folC | 2746819 | c.780T>C | synonymous_variant | 1.0 |
folC | 2746836 | p.Ser255Ala | missense_variant | 1.0 |
folC | 2746837 | c.762G>C | synonymous_variant | 1.0 |
pepQ | 2859432 | c.987T>C | synonymous_variant | 0.67 |
pepQ | 2859438 | c.981T>C | synonymous_variant | 0.67 |
pepQ | 2859468 | c.951G>T | synonymous_variant | 0.67 |
pepQ | 2859471 | c.948A>G | synonymous_variant | 0.67 |
pepQ | 2859486 | c.933A>G | synonymous_variant | 0.67 |
pepQ | 2859489 | p.Val310Ala | missense_variant | 0.67 |
pepQ | 2859492 | c.927G>C | synonymous_variant | 0.67 |
pepQ | 2859498 | c.921C>A | synonymous_variant | 0.67 |
pepQ | 2859510 | c.909T>C | synonymous_variant | 1.0 |
pepQ | 2859513 | c.906A>C | synonymous_variant | 1.0 |
pepQ | 2859525 | c.894T>G | synonymous_variant | 1.0 |
pepQ | 2859528 | c.891T>C | synonymous_variant | 1.0 |
pepQ | 2859534 | c.885A>G | synonymous_variant | 1.0 |
pepQ | 2859539 | c.880C>T | synonymous_variant | 1.0 |
pepQ | 2859540 | c.879A>T | synonymous_variant | 1.0 |
pepQ | 2859546 | c.873T>C | synonymous_variant | 1.0 |
pepQ | 2859552 | p.His289Gln | missense_variant | 0.67 |
pepQ | 2859870 | c.549T>C | synonymous_variant | 1.0 |
pepQ | 2859873 | c.546T>C | synonymous_variant | 1.0 |
pepQ | 2859908 | p.Gln171Glu | missense_variant | 1.0 |
pepQ | 2859909 | c.510G>C | synonymous_variant | 1.0 |
pepQ | 2859918 | c.501A>C | synonymous_variant | 1.0 |
pepQ | 2859921 | c.498C>G | synonymous_variant | 1.0 |
pepQ | 2859924 | c.495G>C | synonymous_variant | 1.0 |
pepQ | 2859942 | c.477C>G | synonymous_variant | 1.0 |
pepQ | 2859950 | c.469T>C | synonymous_variant | 1.0 |
pepQ | 2859951 | c.468C>T | synonymous_variant | 1.0 |
pepQ | 2859966 | c.453T>C | synonymous_variant | 1.0 |
pepQ | 2859972 | c.447A>G | synonymous_variant | 1.0 |
pepQ | 2859975 | c.444A>G | synonymous_variant | 1.0 |
pepQ | 2859984 | c.435A>G | synonymous_variant | 1.0 |
pepQ | 2859987 | c.432A>G | synonymous_variant | 1.0 |
pepQ | 2860001 | p.Leu140Val | missense_variant | 1.0 |
thyA | 3073860 | c.612C>G | synonymous_variant | 1.0 |
thyA | 3073863 | c.609T>C | synonymous_variant | 1.0 |
thyA | 3073874 | p.Ile200Val | missense_variant | 1.0 |
thyA | 3073887 | p.Ser195Gly | missense_variant | 1.0 |
thyA | 3073892 | c.580T>C | synonymous_variant | 1.0 |
thyA | 3073893 | c.579C>A | synonymous_variant | 1.0 |
thyA | 3073908 | p.Met188Ile | missense_variant | 1.0 |
thyA | 3073923 | c.547_549delTTGinsCTA | synonymous_variant | 1.0 |
thyA | 3073929 | c.543T>C | synonymous_variant | 1.0 |
thyA | 3073950 | c.522G>C | synonymous_variant | 1.0 |
thyA | 3073953 | c.519T>C | synonymous_variant | 1.0 |
thyA | 3073956 | c.516G>C | synonymous_variant | 1.0 |
thyA | 3073959 | c.513T>C | synonymous_variant | 1.0 |
thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
fbiB | 3641834 | c.300G>T | synonymous_variant | 0.67 |
fbiB | 3641840 | c.306T>C | synonymous_variant | 0.67 |
fbiB | 3641846 | c.312G>C | synonymous_variant | 1.0 |
fbiB | 3641877 | p.Arg115Ser | missense_variant | 0.75 |
fbiB | 3641880 | p.Ser116Asp | missense_variant | 0.75 |
fbiB | 3641885 | c.351G>A | synonymous_variant | 0.75 |
fbiB | 3641888 | c.354A>G | synonymous_variant | 0.75 |
fbiB | 3641909 | c.375T>C | synonymous_variant | 0.75 |
fbiB | 3641918 | c.384T>C | synonymous_variant | 0.75 |
fbiB | 3641924 | c.390A>G | synonymous_variant | 0.75 |
fbiB | 3641925 | p.Thr131Ala | missense_variant | 0.75 |
fbiB | 3641928 | c.394T>C | synonymous_variant | 0.75 |
fbiB | 3641933 | c.399C>G | synonymous_variant | 0.75 |
fbiB | 3641945 | c.411C>G | synonymous_variant | 0.75 |
fbiB | 3641961 | p.Thr143Asp | missense_variant | 0.75 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 1.0 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 1.0 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 1.0 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 1.0 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 1.0 |
clpC1 | 4038683 | c.2022T>G | synonymous_variant | 1.0 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 1.0 |
clpC1 | 4038710 | c.1995G>C | synonymous_variant | 1.0 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 1.0 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 1.0 |
clpC1 | 4039391 | c.1314T>C | synonymous_variant | 1.0 |
clpC1 | 4039406 | c.1299G>C | synonymous_variant | 1.0 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 1.0 |
clpC1 | 4039412 | c.1293T>C | synonymous_variant | 1.0 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 1.0 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 1.0 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 1.0 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
clpC1 | 4039913 | c.792C>T | synonymous_variant | 0.67 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.5 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.5 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.5 |
embC | 4241050 | c.1188T>G | synonymous_variant | 0.67 |
embC | 4241071 | c.1209C>G | synonymous_variant | 0.67 |
embC | 4241095 | c.1233C>T | synonymous_variant | 0.67 |
embC | 4241107 | c.1245G>C | synonymous_variant | 0.67 |
embC | 4241140 | c.1278A>G | synonymous_variant | 1.0 |
embC | 4241158 | c.1296T>C | synonymous_variant | 1.0 |
embC | 4241161 | c.1299C>G | synonymous_variant | 1.0 |
embC | 4241162 | c.1300T>C | synonymous_variant | 1.0 |
embC | 4241167 | c.1305C>G | synonymous_variant | 1.0 |
embB | 4246292 | c.-222A>G | upstream_gene_variant | 1.0 |
embA | 4246299 | p.Ser1023Ala | missense_variant | 0.67 |
embA | 4246305 | p.Ser1025Glu | missense_variant | 1.0 |
embB | 4246316 | c.-198T>C | upstream_gene_variant | 1.0 |
embB | 4246352 | c.-162G>C | upstream_gene_variant | 0.67 |
embA | 4246359 | p.Ala1043Ser | missense_variant | 1.0 |
embB | 4246373 | c.-141T>C | upstream_gene_variant | 1.0 |
embB | 4246376 | c.-138G>C | upstream_gene_variant | 1.0 |
embB | 4246385 | c.-129T>C | upstream_gene_variant | 0.67 |
embB | 4246400 | c.-114G>C | upstream_gene_variant | 0.67 |
embA | 4246413 | p.His1061Tyr | missense_variant | 1.0 |
embB | 4246419 | c.-95C>T | upstream_gene_variant | 1.0 |
embB | 4247437 | c.924A>G | synonymous_variant | 1.0 |
embB | 4247470 | c.957T>C | synonymous_variant | 1.0 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.75 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.75 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.75 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.75 |
embB | 4247539 | c.1026T>C | synonymous_variant | 0.67 |
embB | 4247550 | p.Ala346Asp | missense_variant | 0.67 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.67 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.67 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.67 |
embB | 4247893 | c.1380C>T | synonymous_variant | 0.67 |
embB | 4247897 | p.Met462Val | missense_variant | 0.67 |
embB | 4247905 | c.1392G>A | synonymous_variant | 1.0 |
embB | 4247914 | c.1401G>C | synonymous_variant | 1.0 |
embB | 4247916 | p.Arg468His | missense_variant | 1.0 |
embB | 4247920 | c.1407T>C | synonymous_variant | 1.0 |
embB | 4247940 | p.Leu476Trp | missense_variant | 1.0 |
embB | 4247945 | c.1432T>C | synonymous_variant | 1.0 |
embB | 4247951 | p.Ser480Ala | missense_variant | 1.0 |
embB | 4247957 | p.Met482Leu | missense_variant | 1.0 |
embB | 4247965 | c.1452C>G | synonymous_variant | 1.0 |
embB | 4247971 | c.1458C>T | synonymous_variant | 1.0 |
embB | 4247972 | p.Thr487Ser | missense_variant | 1.0 |
embB | 4247983 | c.1470G>C | synonymous_variant | 1.0 |
embB | 4248007 | c.1494C>T | synonymous_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269051 | c.-215C>T | upstream_gene_variant | 1.0 |
aftB | 4269060 | c.-224G>C | upstream_gene_variant | 1.0 |
ubiA | 4269075 | p.Ile253Val | missense_variant | 1.0 |