Run ID: SRR6046152
Sample name:
Date: 04-04-2023 12:12:09
Number of reads: 60481
Percentage reads mapped: 1.95
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 | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.6 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.4 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6943 | c.-359G>A | upstream_gene_variant | 1.0 |
gyrA | 6949 | c.-353A>G | upstream_gene_variant | 1.0 |
gyrA | 6952 | c.-350C>G | upstream_gene_variant | 1.0 |
gyrA | 6967 | c.-335T>C | upstream_gene_variant | 1.0 |
gyrA | 6970 | c.-332C>T | upstream_gene_variant | 1.0 |
gyrA | 6973 | c.-329G>C | upstream_gene_variant | 1.0 |
gyrA | 6976 | c.-326A>G | upstream_gene_variant | 1.0 |
gyrA | 6982 | c.-320A>G | upstream_gene_variant | 1.0 |
gyrA | 6994 | c.-308C>T | upstream_gene_variant | 1.0 |
gyrA | 7006 | c.-296T>C | upstream_gene_variant | 1.0 |
gyrA | 7010 | c.-292C>T | upstream_gene_variant | 1.0 |
gyrA | 7021 | c.-281G>A | upstream_gene_variant | 1.0 |
gyrA | 7033 | c.-269G>C | upstream_gene_variant | 1.0 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 1.0 |
gyrA | 7484 | c.183T>C | synonymous_variant | 1.0 |
gyrA | 7490 | c.189C>G | synonymous_variant | 1.0 |
gyrA | 7496 | c.195C>T | synonymous_variant | 1.0 |
gyrA | 7499 | c.198G>C | synonymous_variant | 1.0 |
mshA | 575689 | c.342G>C | synonymous_variant | 1.0 |
mshA | 575695 | c.348C>G | synonymous_variant | 1.0 |
mshA | 575704 | c.357T>C | synonymous_variant | 1.0 |
mshA | 575705 | c.358T>C | synonymous_variant | 1.0 |
mshA | 575713 | c.366G>A | synonymous_variant | 1.0 |
mshA | 575719 | c.372C>T | synonymous_variant | 1.0 |
mshA | 575734 | c.387T>G | synonymous_variant | 1.0 |
mshA | 575779 | c.432A>G | synonymous_variant | 1.0 |
mshA | 575785 | c.438T>C | synonymous_variant | 1.0 |
mshA | 575786 | p.Tyr147His | missense_variant | 1.0 |
rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
rpoB | 760313 | c.507G>C | synonymous_variant | 1.0 |
rpoB | 760424 | c.618C>G | synonymous_variant | 1.0 |
rpoB | 760430 | c.624T>C | synonymous_variant | 1.0 |
rpoB | 760454 | c.648C>G | synonymous_variant | 1.0 |
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 | 761564 | c.1758G>C | synonymous_variant | 1.0 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 1.0 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 1.0 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 1.0 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 1.0 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
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 | 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 | 763633 | c.264T>C | synonymous_variant | 1.0 |
rpoC | 763636 | c.267T>C | synonymous_variant | 1.0 |
rpoC | 763648 | c.279C>A | synonymous_variant | 1.0 |
rpoC | 763714 | c.345G>A | synonymous_variant | 1.0 |
rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
rpoC | 763768 | c.399C>G | synonymous_variant | 1.0 |
rpoC | 763790 | p.Glu141Asn | missense_variant | 1.0 |
rpoC | 763801 | c.432C>G | synonymous_variant | 1.0 |
rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
rpoC | 763813 | c.444C>G | synonymous_variant | 1.0 |
rpoC | 763816 | c.447C>G | synonymous_variant | 1.0 |
rpoC | 763888 | c.519G>T | synonymous_variant | 1.0 |
rpoC | 763894 | c.525A>G | synonymous_variant | 1.0 |
rpoC | 764188 | c.819A>G | synonymous_variant | 1.0 |
rpoC | 764203 | c.834G>C | synonymous_variant | 1.0 |
rpoC | 764206 | p.Asp279Glu | missense_variant | 1.0 |
rpoC | 764217 | p.Asn283Ser | missense_variant | 1.0 |
rpoC | 764245 | c.876C>G | synonymous_variant | 1.0 |
rpoC | 764257 | c.888G>C | synonymous_variant | 1.0 |
rpoC | 764266 | c.897T>C | synonymous_variant | 1.0 |
rpoC | 764269 | c.900G>C | synonymous_variant | 1.0 |
rpoC | 764272 | c.903G>C | synonymous_variant | 1.0 |
rpoC | 764278 | c.909A>G | synonymous_variant | 1.0 |
rpoC | 765612 | p.His748Arg | missense_variant | 1.0 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 1.0 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 1.0 |
rpoC | 765673 | p.Asp768Glu | missense_variant | 1.0 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 1.0 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 1.0 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 1.0 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 1.0 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 1.0 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
rpoC | 766658 | p.Arg1097Gly | missense_variant | 1.0 |
rpoC | 766666 | c.3297C>G | synonymous_variant | 1.0 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 1.0 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 1.0 |
rpoC | 766738 | c.3369G>C | synonymous_variant | 1.0 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 1.0 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 1.0 |
rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
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 | 1.0 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 1.0 |
rplC | 800684 | c.-125G>A | upstream_gene_variant | 1.0 |
rplC | 800690 | c.-119C>G | upstream_gene_variant | 1.0 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
rplC | 800844 | c.36T>C | synonymous_variant | 1.0 |
rplC | 800867 | p.Ser20Asn | missense_variant | 1.0 |
rplC | 800874 | c.66A>G | synonymous_variant | 1.0 |
rplC | 800877 | c.69A>C | synonymous_variant | 1.0 |
rplC | 800880 | c.72A>C | synonymous_variant | 1.0 |
rplC | 800889 | c.81C>G | synonymous_variant | 1.0 |
rplC | 800907 | c.99C>G | synonymous_variant | 1.0 |
rplC | 800916 | c.108A>G | synonymous_variant | 1.0 |
rplC | 800934 | c.126C>G | synonymous_variant | 1.0 |
rplC | 800937 | c.129A>G | synonymous_variant | 1.0 |
rplC | 800946 | c.138T>C | synonymous_variant | 1.0 |
rplC | 800949 | c.141T>C | synonymous_variant | 1.0 |
rplC | 800967 | c.159C>A | synonymous_variant | 1.0 |
rplC | 800970 | c.162T>C | synonymous_variant | 1.0 |
rplC | 800973 | c.165C>T | synonymous_variant | 1.0 |
rplC | 800982 | c.174C>T | synonymous_variant | 1.0 |
rplC | 801004 | p.Leu66Val | missense_variant | 1.0 |
rplC | 801009 | c.201A>C | synonymous_variant | 1.0 |
rplC | 801027 | c.219C>G | synonymous_variant | 1.0 |
rplC | 801039 | c.231A>G | synonymous_variant | 1.0 |
fbiC | 1304115 | c.1185A>G | synonymous_variant | 1.0 |
fbiC | 1304127 | c.1197A>C | synonymous_variant | 1.0 |
fbiC | 1304133 | c.1203G>C | synonymous_variant | 1.0 |
fbiC | 1304136 | c.1206C>G | synonymous_variant | 1.0 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 1.0 |
fbiC | 1304637 | c.1707G>A | synonymous_variant | 1.0 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 1.0 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 1.0 |
fbiC | 1304670 | c.1740G>C | synonymous_variant | 1.0 |
fbiC | 1304671 | p.Val581Thr | missense_variant | 1.0 |
fbiC | 1304675 | p.Gly582Glu | missense_variant | 1.0 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 1.0 |
fbiC | 1304694 | c.1764A>C | synonymous_variant | 1.0 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 1.0 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 1.0 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 1.0 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 1.0 |
fbiC | 1304742 | c.1812T>G | synonymous_variant | 1.0 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 1.0 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 1.0 |
fbiC | 1304778 | c.1848T>C | synonymous_variant | 1.0 |
fbiC | 1304784 | c.1854T>G | synonymous_variant | 1.0 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 1.0 |
fbiC | 1304799 | c.1869G>C | synonymous_variant | 1.0 |
fbiC | 1305215 | p.Ser762Thr | missense_variant | 1.0 |
fbiC | 1305228 | c.2298C>T | synonymous_variant | 1.0 |
fbiC | 1305231 | c.2301C>G | synonymous_variant | 1.0 |
fbiC | 1305237 | c.2307A>G | synonymous_variant | 1.0 |
fbiC | 1305243 | c.2313T>C | synonymous_variant | 1.0 |
fbiC | 1305244 | c.2314T>C | synonymous_variant | 1.0 |
fbiC | 1305273 | c.2343C>T | synonymous_variant | 1.0 |
fbiC | 1305276 | c.2346G>C | synonymous_variant | 1.0 |
fbiC | 1305282 | c.2352T>C | synonymous_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472135 | n.290C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472279 | n.434T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472349 | n.504A>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472374 | n.529T>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472415 | n.570T>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472418 | n.573T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472553 | n.708C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472572 | n.727T>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472574 | n.729T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472582 | n.738_739delTA | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472594 | n.749G>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472836 | n.991G>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472838 | n.993A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472841 | n.996G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472845 | n.1000G>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472846 | n.1001C>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472861 | n.1016G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472874 | n.1029C>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472877 | n.1032T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472880 | n.1035_1036insA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472912 | n.1067C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472917 | n.1072G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473009 | n.1165delC | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473198 | n.1354delC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473290 | n.1445C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474275 | n.618T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475538 | n.1881T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475540 | n.1883C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475550 | n.1893A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475551 | n.1894T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475555 | n.1898T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475564 | n.1907C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475574 | n.1917C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475575 | n.1918C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475576 | n.1919C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475717 | n.2060C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475877 | n.2220C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475878 | n.2221T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475879 | n.2222T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476196 | n.2539C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476210 | n.2553G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476214 | n.2557G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.67 |
inhA | 1674243 | c.42A>G | synonymous_variant | 1.0 |
inhA | 1674249 | c.48C>T | synonymous_variant | 1.0 |
inhA | 1674279 | c.78A>G | synonymous_variant | 1.0 |
inhA | 1674285 | c.84A>G | synonymous_variant | 1.0 |
inhA | 1674300 | c.99C>G | synonymous_variant | 1.0 |
inhA | 1674304 | p.Gln35Glu | missense_variant | 1.0 |
inhA | 1674315 | c.114C>G | synonymous_variant | 1.0 |
inhA | 1674342 | c.141T>C | synonymous_variant | 1.0 |
inhA | 1674352 | p.Thr51Ala | missense_variant | 1.0 |
inhA | 1674387 | c.186A>G | 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 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 1.0 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 1.0 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 1.0 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
rpsA | 1834558 | c.1017C>G | synonymous_variant | 1.0 |
ndh | 2102830 | c.213G>C | synonymous_variant | 1.0 |
ndh | 2102842 | c.201A>G | synonymous_variant | 1.0 |
ndh | 2102857 | c.186T>C | synonymous_variant | 1.0 |
ndh | 2102866 | c.177C>T | synonymous_variant | 1.0 |
ndh | 2102872 | c.171A>G | synonymous_variant | 1.0 |
ndh | 2102883 | c.160C>T | synonymous_variant | 1.0 |
ndh | 2102884 | c.159G>A | synonymous_variant | 1.0 |
kasA | 2518627 | c.513T>C | synonymous_variant | 1.0 |
kasA | 2518642 | c.528A>G | synonymous_variant | 1.0 |
kasA | 2518645 | c.531G>C | synonymous_variant | 1.0 |
kasA | 2518663 | c.549T>C | synonymous_variant | 1.0 |
kasA | 2518672 | c.558G>C | synonymous_variant | 1.0 |
kasA | 2518678 | c.564C>T | synonymous_variant | 1.0 |
kasA | 2518681 | c.567C>T | synonymous_variant | 1.0 |
kasA | 2518684 | c.570C>G | synonymous_variant | 1.0 |
kasA | 2518697 | p.Cys195Ala | missense_variant | 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 |
folC | 2747023 | c.576C>G | synonymous_variant | 1.0 |
folC | 2747032 | c.567A>G | synonymous_variant | 1.0 |
folC | 2747036 | p.Asn188Ser | missense_variant | 1.0 |
folC | 2747059 | c.540T>G | synonymous_variant | 1.0 |
folC | 2747062 | c.537A>T | synonymous_variant | 1.0 |
folC | 2747070 | p.Met177Leu | missense_variant | 1.0 |
folC | 2747074 | c.525G>C | synonymous_variant | 1.0 |
folC | 2747086 | c.513A>G | synonymous_variant | 1.0 |
folC | 2747089 | c.510G>C | synonymous_variant | 1.0 |
folC | 2747778 | c.-180T>C | upstream_gene_variant | 1.0 |
folC | 2747790 | c.-192G>C | upstream_gene_variant | 1.0 |
folC | 2747798 | c.-200A>C | upstream_gene_variant | 1.0 |
pepQ | 2859306 | c.1113T>C | synonymous_variant | 1.0 |
pepQ | 2859318 | c.1101A>G | synonymous_variant | 1.0 |
pepQ | 2859335 | c.1084T>C | synonymous_variant | 1.0 |
thyX | 3067673 | c.273C>T | synonymous_variant | 1.0 |
thyA | 3074307 | c.165A>G | synonymous_variant | 1.0 |
thyA | 3074313 | c.159A>G | synonymous_variant | 1.0 |
thyA | 3074322 | c.150C>G | synonymous_variant | 1.0 |
thyA | 3074325 | c.147A>G | synonymous_variant | 1.0 |
thyA | 3074334 | c.138T>C | synonymous_variant | 1.0 |
thyA | 3074349 | c.123T>C | synonymous_variant | 1.0 |
thyA | 3074360 | c.112T>C | synonymous_variant | 1.0 |
thyA | 3074361 | c.111T>C | synonymous_variant | 1.0 |
ald | 3087233 | c.414T>C | synonymous_variant | 1.0 |
ald | 3087236 | c.417A>G | synonymous_variant | 1.0 |
ald | 3087240 | p.Ala141Ser | missense_variant | 1.0 |
ald | 3087251 | c.432T>C | synonymous_variant | 1.0 |
ald | 3087254 | c.435C>G | synonymous_variant | 1.0 |
ald | 3087257 | c.438T>C | synonymous_variant | 1.0 |
ald | 3087260 | c.441C>T | synonymous_variant | 1.0 |
ald | 3087272 | c.453A>G | synonymous_variant | 1.0 |
ald | 3087281 | c.462G>C | synonymous_variant | 1.0 |
ald | 3087284 | c.465C>G | synonymous_variant | 1.0 |
ald | 3087290 | c.471T>C | synonymous_variant | 1.0 |
ald | 3087311 | c.492C>G | synonymous_variant | 1.0 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 1.0 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 1.0 |
rpoA | 3877770 | c.738A>T | synonymous_variant | 1.0 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 1.0 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 1.0 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 1.0 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 1.0 |
rpoA | 3878409 | c.99C>G | synonymous_variant | 1.0 |
rpoA | 3878430 | c.78G>T | synonymous_variant | 1.0 |
rpoA | 3878442 | c.66G>C | synonymous_variant | 1.0 |
rpoA | 3878454 | c.54A>G | synonymous_variant | 1.0 |
rpoA | 3878472 | p.Asp12Glu | missense_variant | 1.0 |
rpoA | 3878480 | p.Ser10Ala | missense_variant | 1.0 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 1.0 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 1.0 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 1.0 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 1.0 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 1.0 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 1.0 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 1.0 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 1.0 |
clpC1 | 4039823 | c.882T>C | synonymous_variant | 1.0 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 1.0 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 1.0 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 1.0 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 1.0 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 1.0 |
embC | 4240780 | c.918T>C | synonymous_variant | 1.0 |
embC | 4240783 | c.921G>C | synonymous_variant | 1.0 |
embC | 4240786 | c.924C>T | synonymous_variant | 1.0 |
embC | 4240789 | c.927T>C | synonymous_variant | 1.0 |
embC | 4240807 | c.945C>T | synonymous_variant | 1.0 |
embC | 4240816 | c.954C>T | synonymous_variant | 1.0 |
embC | 4240819 | c.957A>G | synonymous_variant | 1.0 |
embC | 4240828 | c.966G>C | synonymous_variant | 1.0 |
embC | 4240831 | c.969T>G | synonymous_variant | 1.0 |
embC | 4240858 | c.996G>C | synonymous_variant | 1.0 |
embC | 4240867 | c.1005T>A | synonymous_variant | 1.0 |
embC | 4240870 | c.1008T>C | synonymous_variant | 1.0 |
embC | 4240879 | c.1017G>C | synonymous_variant | 1.0 |
embC | 4240885 | c.1023T>C | synonymous_variant | 1.0 |
embC | 4240911 | p.Ala350Val | missense_variant | 1.0 |
embC | 4240921 | c.1059C>G | synonymous_variant | 1.0 |
embC | 4240936 | c.1074A>G | synonymous_variant | 1.0 |
embC | 4241002 | c.1140G>C | synonymous_variant | 1.0 |
embC | 4241140 | c.1278A>G | synonymous_variant | 1.0 |
embA | 4244918 | c.1686G>A | synonymous_variant | 1.0 |
embA | 4244921 | c.1689C>G | synonymous_variant | 1.0 |
embA | 4244933 | c.1701A>G | synonymous_variant | 1.0 |
embA | 4244936 | c.1704C>G | synonymous_variant | 1.0 |
embA | 4244970 | p.Leu580Val | missense_variant | 1.0 |
embB | 4246280 | c.-234G>C | upstream_gene_variant | 1.0 |
embB | 4246292 | c.-222A>G | upstream_gene_variant | 1.0 |
embA | 4246299 | p.Ser1023Ala | missense_variant | 1.0 |
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 | 1.0 |
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 | 1.0 |
embB | 4246400 | c.-114G>C | upstream_gene_variant | 1.0 |
embA | 4246413 | p.His1061Tyr | missense_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 | 1.0 |
embB | 4247497 | c.984T>C | synonymous_variant | 1.0 |
embB | 4247500 | c.987C>G | synonymous_variant | 1.0 |
embB | 4247512 | c.999T>C | synonymous_variant | 1.0 |
embB | 4247539 | c.1026T>C | synonymous_variant | 1.0 |
embB | 4247550 | p.Ala346Asp | missense_variant | 1.0 |
embB | 4247554 | c.1041T>C | synonymous_variant | 1.0 |
embB | 4249543 | c.3030G>C | synonymous_variant | 1.0 |
embB | 4249558 | c.3045A>C | synonymous_variant | 1.0 |
embB | 4249573 | c.3060T>C | synonymous_variant | 1.0 |
embB | 4249580 | p.Leu1023Met | missense_variant | 1.0 |
embB | 4249594 | c.3081G>C | synonymous_variant | 1.0 |
embB | 4249600 | c.3087A>G | synonymous_variant | 1.0 |
embB | 4249609 | c.3096T>C | synonymous_variant | 1.0 |
aftB | 4269153 | c.-317C>G | upstream_gene_variant | 1.0 |
aftB | 4269261 | c.-425G>A | upstream_gene_variant | 1.0 |
aftB | 4269282 | c.-446G>A | upstream_gene_variant | 1.0 |
aftB | 4269285 | c.-449T>G | upstream_gene_variant | 1.0 |
aftB | 4269291 | c.-455A>C | upstream_gene_variant | 1.0 |