Run ID: SRR13861153
Sample name:
Date: 03-04-2023 09:24:51
Number of reads: 1123950
Percentage reads mapped: 37.5
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247448 | p.His312Arg | missense_variant | 0.15 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.24 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.24 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.22 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.21 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.21 |
gyrB | 6299 | c.1060C>T | synonymous_variant | 0.22 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.22 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.2 |
gyrA | 6325 | c.-977C>G | upstream_gene_variant | 0.2 |
gyrA | 6361 | c.-941G>A | upstream_gene_variant | 0.14 |
gyrA | 6379 | c.-923C>G | upstream_gene_variant | 0.15 |
gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.15 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.17 |
gyrA | 7835 | c.534A>G | synonymous_variant | 0.15 |
gyrA | 7838 | c.537C>G | synonymous_variant | 0.16 |
gyrA | 8069 | c.768T>C | synonymous_variant | 0.15 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.17 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.16 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.18 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.18 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.2 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.22 |
gyrA | 8204 | c.903C>T | synonymous_variant | 0.22 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.22 |
gyrA | 8216 | c.915G>A | synonymous_variant | 0.21 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.2 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.19 |
gyrA | 8234 | c.933T>G | synonymous_variant | 0.19 |
gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 0.18 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.2 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.18 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.18 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.19 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.16 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.16 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.16 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.16 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.15 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.14 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.13 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.16 |
gyrA | 9278 | c.1977G>C | synonymous_variant | 0.15 |
gyrA | 9281 | c.1980C>G | synonymous_variant | 0.14 |
gyrA | 9291 | c.1990C>T | synonymous_variant | 0.15 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.14 |
fgd1 | 491043 | c.261T>A | synonymous_variant | 0.18 |
fgd1 | 491049 | c.267T>C | synonymous_variant | 0.16 |
fgd1 | 491063 | p.Gly94Ala | missense_variant | 0.17 |
fgd1 | 491077 | p.Asn99Gly | missense_variant | 0.17 |
fgd1 | 491082 | c.300T>C | synonymous_variant | 0.17 |
fgd1 | 491083 | p.Val101Ile | missense_variant | 0.14 |
fgd1 | 491091 | c.309T>C | synonymous_variant | 0.17 |
fgd1 | 491094 | c.312C>G | synonymous_variant | 0.16 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.16 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.21 |
fgd1 | 491137 | p.Glu119Gln | missense_variant | 0.2 |
fgd1 | 491144 | p.Ala121Glu | missense_variant | 0.2 |
fgd1 | 491166 | c.384G>C | synonymous_variant | 0.17 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.14 |
mshA | 575623 | c.276C>G | synonymous_variant | 0.16 |
mshA | 575638 | c.291T>C | synonymous_variant | 0.15 |
mshA | 575641 | c.294A>G | synonymous_variant | 0.15 |
mshA | 575648 | p.Val101Gln | missense_variant | 0.17 |
mshA | 575659 | c.312A>G | synonymous_variant | 0.22 |
mshA | 575665 | c.318G>C | synonymous_variant | 0.26 |
mshA | 575689 | c.342G>C | synonymous_variant | 0.19 |
mshA | 575695 | c.348C>G | synonymous_variant | 0.19 |
mshA | 575704 | c.357T>C | synonymous_variant | 0.17 |
mshA | 575705 | c.358T>C | synonymous_variant | 0.17 |
mshA | 575713 | c.366G>A | synonymous_variant | 0.18 |
mshA | 575719 | c.372C>T | synonymous_variant | 0.19 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.18 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.19 |
mshA | 575746 | c.399C>G | synonymous_variant | 0.22 |
mshA | 575752 | c.405G>A | synonymous_variant | 0.21 |
mshA | 575767 | c.420G>A | synonymous_variant | 0.19 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.19 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.18 |
ccsA | 620257 | p.Ile123Val | missense_variant | 0.14 |
ccsA | 620269 | p.Val127Ile | missense_variant | 0.14 |
ccsA | 620283 | c.393T>C | synonymous_variant | 0.13 |
ccsA | 620288 | p.Arg133Gln | missense_variant | 0.14 |
ccsA | 620661 | c.771C>G | synonymous_variant | 0.16 |
ccsA | 620703 | c.813G>C | synonymous_variant | 0.21 |
ccsA | 620710 | p.Val274Ile | missense_variant | 0.2 |
ccsA | 620718 | c.828G>C | synonymous_variant | 0.2 |
ccsA | 620721 | c.831G>C | synonymous_variant | 0.2 |
ccsA | 620730 | c.840C>T | synonymous_variant | 0.2 |
ccsA | 620733 | c.843G>C | synonymous_variant | 0.2 |
ccsA | 620734 | c.844C>A | synonymous_variant | 0.2 |
ccsA | 620739 | c.849A>G | synonymous_variant | 0.2 |
ccsA | 620745 | c.855G>C | synonymous_variant | 0.19 |
ccsA | 620748 | c.858T>A | synonymous_variant | 0.18 |
ccsA | 620778 | c.888T>C | synonymous_variant | 0.18 |
ccsA | 620784 | c.894C>G | synonymous_variant | 0.17 |
ccsA | 620787 | c.897C>G | synonymous_variant | 0.16 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.15 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.15 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.16 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.18 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.17 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.21 |
rpoB | 760307 | c.501T>C | synonymous_variant | 0.18 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.18 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.17 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.18 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.17 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.17 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.17 |
rpoB | 760418 | c.612G>C | synonymous_variant | 0.17 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.19 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.19 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.21 |
rpoB | 760514 | c.708C>T | synonymous_variant | 0.19 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.2 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.18 |
rpoB | 760533 | p.Val243Thr | missense_variant | 0.18 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.16 |
rpoB | 760563 | p.Arg253Met | missense_variant | 0.15 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.17 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.18 |
rpoB | 760928 | c.1122G>C | synonymous_variant | 0.16 |
rpoB | 760934 | c.1128C>T | synonymous_variant | 0.18 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.17 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.15 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.15 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.17 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.17 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 0.15 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.14 |
rpoB | 761657 | c.1851C>G | synonymous_variant | 0.18 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.16 |
rpoB | 761687 | c.1881C>T | synonymous_variant | 0.14 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 0.14 |
rpoB | 761847 | p.Cys681Ser | missense_variant | 0.13 |
rpoB | 761858 | c.2052G>C | synonymous_variant | 0.15 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.15 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.16 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.18 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.16 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.16 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.16 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.16 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.15 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.14 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.14 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.14 |
rpoB | 762027 | c.2221_2223delCTCinsTTG | synonymous_variant | 0.14 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.14 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.15 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.15 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.17 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.15 |
rpoB | 762218 | c.2412T>G | synonymous_variant | 0.16 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.16 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.18 |
rpoB | 762489 | p.Val895Gln | missense_variant | 0.18 |
rpoC | 762551 | c.-819C>T | upstream_gene_variant | 0.15 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.17 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.17 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.16 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.16 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.17 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.18 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.15 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.18 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.16 |
rpoC | 763158 | c.-212C>T | upstream_gene_variant | 0.14 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.14 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.14 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.17 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.18 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.18 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.17 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.18 |
rpoC | 763658 | c.289_291delCTTinsTTG | synonymous_variant | 0.15 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.15 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.16 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.16 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.15 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.14 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.14 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.16 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.16 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.16 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.16 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.15 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.15 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.17 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.15 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.15 |
rpoC | 764389 | p.Leu340Phe | missense_variant | 0.14 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.17 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.18 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.16 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.17 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.15 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.15 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.15 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.15 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.13 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.14 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.14 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.16 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.15 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.14 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.14 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.17 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.18 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.18 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.18 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.15 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.17 |
rpoC | 765739 | c.2370G>C | synonymous_variant | 0.18 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.17 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.16 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.14 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.18 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.18 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.22 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.22 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.22 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.2 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.21 |
rpoC | 765928 | c.2559C>G | synonymous_variant | 0.18 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.13 |
rpoC | 765970 | c.2601C>T | synonymous_variant | 0.13 |
rpoC | 766010 | p.Ser881Thr | missense_variant | 0.12 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.13 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.14 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.14 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.15 |
rpoC | 766531 | c.3162G>T | synonymous_variant | 0.15 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.12 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.15 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.16 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.14 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.17 |
rpoC | 766978 | c.3609C>G | synonymous_variant | 0.16 |
rpoC | 767009 | p.Ser1214Thr | missense_variant | 0.13 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.16 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.15 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.14 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.14 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.15 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.14 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.16 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.19 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.15 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.15 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.17 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.18 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.18 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.17 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.16 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.15 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.15 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.15 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.15 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.2 |
rplC | 800867 | p.Ser20Asn | missense_variant | 0.23 |
rplC | 800874 | c.66A>G | synonymous_variant | 0.21 |
rplC | 800877 | c.69A>C | synonymous_variant | 0.2 |
rplC | 800880 | c.72A>G | synonymous_variant | 0.22 |
rplC | 800889 | c.81C>G | synonymous_variant | 0.2 |
rplC | 800907 | c.99C>G | synonymous_variant | 0.16 |
rplC | 800916 | c.108A>G | synonymous_variant | 0.16 |
rplC | 800937 | c.129A>G | synonymous_variant | 0.15 |
rplC | 800939 | p.Arg44His | missense_variant | 0.14 |
rplC | 800946 | c.138T>C | synonymous_variant | 0.15 |
rplC | 800949 | c.141T>C | synonymous_variant | 0.15 |
rplC | 800955 | c.147C>G | synonymous_variant | 0.15 |
rplC | 800967 | c.159C>G | synonymous_variant | 0.15 |
rplC | 800970 | c.162T>C | synonymous_variant | 0.15 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.16 |
fbiC | 1303638 | c.708A>G | synonymous_variant | 0.16 |
fbiC | 1303686 | c.756C>G | synonymous_variant | 0.21 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 0.18 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 0.16 |
fbiC | 1303728 | c.798G>A | synonymous_variant | 0.16 |
fbiC | 1303730 | p.Leu267Pro | missense_variant | 0.16 |
fbiC | 1303732 | p.Ser268Ala | missense_variant | 0.15 |
fbiC | 1303737 | c.807G>A | synonymous_variant | 0.15 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.13 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.22 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.22 |
fbiC | 1303920 | c.990C>G | synonymous_variant | 0.21 |
fbiC | 1303923 | c.993C>T | synonymous_variant | 0.21 |
fbiC | 1303929 | c.999G>C | synonymous_variant | 0.21 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.19 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.19 |
fbiC | 1303969 | p.Val347Ile | missense_variant | 0.19 |
fbiC | 1303973 | p.Gly348Ala | missense_variant | 0.17 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.15 |
fbiC | 1304001 | c.1071C>G | synonymous_variant | 0.15 |
fbiC | 1304034 | c.1104A>G | synonymous_variant | 0.18 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.17 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.17 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.16 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.16 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.15 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.16 |
fbiC | 1304754 | c.1824G>A | synonymous_variant | 0.16 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.17 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.15 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.15 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.15 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.14 |
fbiC | 1305297 | c.2367G>C | synonymous_variant | 0.15 |
fbiC | 1305300 | c.2370A>G | synonymous_variant | 0.16 |
fbiC | 1305303 | c.2373T>C | synonymous_variant | 0.16 |
fbiC | 1305311 | p.Arg794Gln | missense_variant | 0.17 |
fbiC | 1305331 | p.Glu801Asn | missense_variant | 0.17 |
fbiC | 1305336 | c.2406T>C | synonymous_variant | 0.16 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474104 | n.447G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475273 | n.1616T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.21 |
rpsA | 1833851 | p.Lys104Gln | missense_variant | 0.95 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.16 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.16 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.16 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.15 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.15 |
rpsA | 1834558 | c.1017C>G | synonymous_variant | 0.17 |
rpsA | 1834606 | c.1065C>G | synonymous_variant | 0.14 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.15 |
rpsA | 1834688 | c.1147_1149delAGTinsTCC | synonymous_variant | 0.15 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.19 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 0.19 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.19 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.2 |
rpsA | 1834780 | c.1239A>G | synonymous_variant | 0.2 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.19 |
rpsA | 1834789 | c.1248T>C | synonymous_variant | 0.17 |
rpsA | 1834792 | c.1251G>C | synonymous_variant | 0.15 |
Rv1979c | 2223241 | c.-77C>G | upstream_gene_variant | 1.0 |
pncA | 2289811 | c.-570C>T | upstream_gene_variant | 1.0 |
pncA | 2289994 | c.-753A>C | upstream_gene_variant | 1.0 |
kasA | 2518301 | p.His63Asp | missense_variant | 1.0 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.15 |
kasA | 2519095 | c.981C>G | synonymous_variant | 0.15 |
kasA | 2519104 | c.990T>A | synonymous_variant | 0.15 |
kasA | 2519108 | p.Asp332Gln | missense_variant | 0.15 |
kasA | 2519111 | p.Gln333Glu | missense_variant | 0.14 |
kasA | 2519125 | c.1011C>T | synonymous_variant | 0.14 |
kasA | 2519146 | c.1032C>A | synonymous_variant | 0.14 |
kasA | 2519167 | c.1053T>C | synonymous_variant | 0.14 |
kasA | 2519173 | c.1059C>G | synonymous_variant | 0.14 |
kasA | 2519176 | c.1062G>A | synonymous_variant | 0.14 |
kasA | 2519197 | c.1083G>C | synonymous_variant | 0.16 |
pepQ | 2859859 | p.Ala187Glu | missense_variant | 1.0 |
Rv2752c | 3064886 | p.Ala436Pro | missense_variant | 0.97 |
Rv2752c | 3065258 | p.Met312Val | missense_variant | 1.0 |
Rv2752c | 3066002 | p.Met64Leu | missense_variant | 0.18 |
thyX | 3067376 | c.570G>C | synonymous_variant | 0.15 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.17 |
thyX | 3067451 | c.495G>A | synonymous_variant | 0.15 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.15 |
thyX | 3067463 | p.Ile161Val | missense_variant | 0.16 |
thyX | 3067466 | c.480G>C | synonymous_variant | 0.16 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.17 |
thyX | 3067500 | p.Lys149Arg | missense_variant | 0.16 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.17 |
thyX | 3067531 | p.Ala139Thr | missense_variant | 0.12 |
thyX | 3067619 | c.327A>C | synonymous_variant | 0.15 |
thyX | 3067718 | c.228C>G | synonymous_variant | 0.17 |
thyX | 3067721 | c.225T>C | synonymous_variant | 0.17 |
thyX | 3067724 | c.222G>A | synonymous_variant | 0.18 |
thyX | 3067727 | c.219A>C | synonymous_variant | 0.18 |
thyX | 3067739 | c.207T>C | synonymous_variant | 0.18 |
thyX | 3067742 | c.204A>C | synonymous_variant | 0.18 |
thyX | 3067761 | p.Arg62Lys | missense_variant | 0.15 |
thyX | 3067765 | p.Leu61Ile | missense_variant | 0.15 |
thyX | 3067781 | c.165C>G | synonymous_variant | 0.17 |
thyX | 3067787 | c.159G>A | synonymous_variant | 0.18 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.18 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.17 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.17 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.17 |
thyX | 3067826 | c.120C>G | synonymous_variant | 0.17 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.15 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.2 |
thyA | 3073926 | c.546G>C | synonymous_variant | 0.19 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.19 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.16 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.2 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.19 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.17 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.18 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.19 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.17 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.17 |
thyA | 3074056 | p.Glu139Ala | missense_variant | 0.16 |
Rv3083 | 3449104 | p.Pro201Ala | missense_variant | 1.0 |
Rv3236c | 3612337 | c.779delG | frameshift_variant | 1.0 |
fbiB | 3641723 | c.189T>C | synonymous_variant | 1.0 |
rpoA | 3877740 | c.768G>T | synonymous_variant | 0.87 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.15 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.15 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.17 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.16 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.14 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.17 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.18 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.17 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.15 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.15 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.15 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.17 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.16 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.22 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.22 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.24 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.22 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.22 |
rpoA | 3878082 | c.426T>C | synonymous_variant | 0.24 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 0.24 |
rpoA | 3878100 | c.408C>G | synonymous_variant | 0.26 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.23 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.23 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.23 |
rpoA | 3878141 | p.Met123Leu | missense_variant | 0.2 |
rpoA | 3878142 | p.Gly122Glu | missense_variant | 0.2 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.2 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.2 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.19 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.18 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.15 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.18 |
rpoA | 3878220 | c.288C>T | synonymous_variant | 0.16 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.14 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.14 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.16 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.14 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.15 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.16 |
clpC1 | 4038434 | c.2271G>C | synonymous_variant | 0.16 |
clpC1 | 4038461 | p.Ala748Asp | missense_variant | 0.14 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.17 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.21 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.19 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.23 |
clpC1 | 4038611 | c.2094C>T | synonymous_variant | 0.2 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.2 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.21 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.14 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.14 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.15 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.16 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.14 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.16 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.16 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.15 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.18 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.16 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.15 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.16 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.15 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.14 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.15 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.14 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.14 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.15 |
clpC1 | 4039208 | c.1497C>G | synonymous_variant | 0.17 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.15 |
clpC1 | 4039268 | c.1437C>G | synonymous_variant | 0.16 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.16 |
clpC1 | 4039286 | c.1419T>C | synonymous_variant | 0.17 |
clpC1 | 4039289 | c.1416T>C | synonymous_variant | 0.16 |
clpC1 | 4039295 | c.1410A>C | synonymous_variant | 0.16 |
clpC1 | 4039298 | c.1407T>C | synonymous_variant | 0.16 |
clpC1 | 4039319 | c.1386T>C | synonymous_variant | 0.19 |
clpC1 | 4039322 | c.1383T>C | synonymous_variant | 0.19 |
clpC1 | 4039328 | c.1377A>G | synonymous_variant | 0.17 |
clpC1 | 4039334 | c.1371G>C | synonymous_variant | 0.16 |
clpC1 | 4039338 | p.Thr456Lys | missense_variant | 0.14 |
clpC1 | 4039388 | c.1317C>A | synonymous_variant | 0.13 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.17 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.17 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.17 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.18 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.18 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.18 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.19 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.23 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.22 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.19 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.21 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.21 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.22 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.26 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.25 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.24 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.2 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.2 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.21 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.18 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.17 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.15 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.17 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.19 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.19 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.19 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.22 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.23 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.25 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.27 |
clpC1 | 4039996 | p.Glu237Gln | missense_variant | 0.24 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.27 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.27 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.24 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.26 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.2 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.21 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.23 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.14 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.16 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.14 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.14 |
embC | 4240216 | c.354T>C | synonymous_variant | 0.15 |
embC | 4240229 | p.Leu123Met | missense_variant | 0.14 |
embC | 4240233 | p.Gln124Leu | missense_variant | 0.14 |
embC | 4240632 | p.Met257Thr | missense_variant | 0.15 |
embC | 4240645 | c.783G>C | synonymous_variant | 0.17 |
embC | 4240654 | c.792C>T | synonymous_variant | 0.18 |
embC | 4240657 | c.795G>C | synonymous_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.15 |
embC | 4241005 | c.1143G>T | synonymous_variant | 0.93 |
embC | 4241081 | c.1220delT | frameshift_variant | 0.88 |
embC | 4242746 | p.Pro962Ser | missense_variant | 1.0 |
embA | 4243969 | p.Val246Ala | missense_variant | 1.0 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.15 |
embB | 4248118 | c.1605T>C | synonymous_variant | 0.22 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.2 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.17 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.16 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.16 |
embB | 4248157 | c.1644A>G | synonymous_variant | 0.16 |
embB | 4248206 | p.Ser565Gly | missense_variant | 0.18 |
embB | 4248220 | c.1707A>G | synonymous_variant | 0.19 |
embB | 4248241 | c.1728C>T | synonymous_variant | 0.21 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.14 |
embB | 4249483 | c.2970C>G | synonymous_variant | 0.16 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.15 |
embB | 4249487 | c.2974T>C | synonymous_variant | 0.15 |
embB | 4249521 | p.Ala1003Val | missense_variant | 0.18 |
embB | 4249525 | c.3012T>C | synonymous_variant | 0.18 |
embB | 4249528 | c.3015C>G | synonymous_variant | 0.18 |
embB | 4249529 | p.Ile1006Val | missense_variant | 0.18 |
embB | 4249532 | p.Ala1007Thr | missense_variant | 0.17 |
embB | 4249537 | c.3024A>G | synonymous_variant | 0.19 |
embB | 4249543 | c.3030G>C | synonymous_variant | 0.19 |
embB | 4249558 | c.3045A>C | synonymous_variant | 0.2 |
embB | 4249564 | c.3051C>T | synonymous_variant | 0.2 |
embB | 4249568 | p.Ser1019Thr | missense_variant | 0.2 |
embB | 4249573 | c.3060T>C | synonymous_variant | 0.18 |
embB | 4249580 | p.Leu1023Met | missense_variant | 0.18 |
embB | 4249594 | c.3081G>C | synonymous_variant | 0.16 |
aftB | 4269183 | c.-347T>C | upstream_gene_variant | 0.15 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.16 |
aftB | 4269222 | c.-386T>G | upstream_gene_variant | 0.16 |
aftB | 4269225 | c.-389C>G | upstream_gene_variant | 0.16 |
aftB | 4269231 | c.-395C>G | upstream_gene_variant | 0.16 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.16 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.15 |
ubiA | 4269271 | p.Val188Ala | missense_variant | 0.15 |