Run ID: ERR473367
Sample name:
Date: 01-04-2023 06:38:54
Number of reads: 35903
Percentage reads mapped: 1.16
Strain: lineage4.9
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5763 | p.Ala175Val | missense_variant | 1.0 |
gyrA | 7018 | c.-284G>C | upstream_gene_variant | 1.0 |
gyrA | 7021 | c.-281G>T | upstream_gene_variant | 1.0 |
gyrB | 7025 | p.Lys596Ala | missense_variant | 1.0 |
gyrA | 7033 | c.-269G>T | upstream_gene_variant | 1.0 |
gyrB | 7051 | p.Glu604Asp | missense_variant | 1.0 |
gyrB | 7058 | p.Ile607Val | missense_variant | 1.0 |
gyrA | 7066 | c.-236G>C | upstream_gene_variant | 1.0 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.67 |
gyrA | 8273 | c.972C>G | synonymous_variant | 0.67 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.67 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.67 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.67 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.67 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.67 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.67 |
rpoB | 760172 | c.366G>C | synonymous_variant | 1.0 |
rpoB | 760181 | c.375T>A | synonymous_variant | 1.0 |
rpoB | 760184 | c.378A>G | synonymous_variant | 1.0 |
rpoB | 760193 | c.387C>G | synonymous_variant | 1.0 |
rpoB | 760199 | c.393C>G | synonymous_variant | 1.0 |
rpoB | 760206 | p.Ile134Val | missense_variant | 0.4 |
rpoB | 760233 | c.427_429delAGTinsTCG | synonymous_variant | 1.0 |
rpoB | 760244 | c.438G>C | synonymous_variant | 1.0 |
rpoB | 760256 | c.450C>T | synonymous_variant | 1.0 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 1.0 |
rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
rpoB | 760313 | c.507G>C | synonymous_variant | 1.0 |
rpoB | 760317 | c.511_513delAGCinsTCG | synonymous_variant | 1.0 |
rpoB | 760331 | c.525G>C | synonymous_variant | 1.0 |
rpoB | 760337 | c.531C>G | synonymous_variant | 1.0 |
rpoB | 760340 | c.534G>T | synonymous_variant | 1.0 |
rpoB | 760356 | p.Thr184Ser | missense_variant | 1.0 |
rpoB | 760361 | c.555T>C | synonymous_variant | 1.0 |
rpoB | 760433 | c.627C>T | synonymous_variant | 1.0 |
rpoB | 760457 | c.651C>T | synonymous_variant | 1.0 |
rpoB | 760463 | c.657C>T | synonymous_variant | 1.0 |
rpoB | 760469 | c.663C>T | synonymous_variant | 1.0 |
rpoB | 760475 | c.669A>G | synonymous_variant | 1.0 |
rpoB | 760478 | c.672C>T | synonymous_variant | 1.0 |
rpoB | 760481 | c.675G>T | synonymous_variant | 1.0 |
rpoB | 760484 | c.678A>G | synonymous_variant | 1.0 |
rpoB | 760502 | c.696C>G | synonymous_variant | 1.0 |
rpoB | 760515 | p.Trp237Met | missense_variant | 0.75 |
rpoB | 760522 | p.Ser239Thr | missense_variant | 1.0 |
rpoB | 760527 | p.Gln241Glu | missense_variant | 1.0 |
rpoB | 760532 | c.726T>C | synonymous_variant | 1.0 |
rpoB | 760533 | p.Val243Thr | missense_variant | 1.0 |
rpoB | 760547 | c.741G>T | synonymous_variant | 1.0 |
rpoB | 760564 | p.Arg253Leu | missense_variant | 1.0 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.67 |
rpoB | 760591 | p.Val262Ala | missense_variant | 1.0 |
rpoB | 760611 | c.805_807delTTGinsCTC | synonymous_variant | 1.0 |
rpoB | 760646 | c.840C>G | synonymous_variant | 1.0 |
rpoB | 760655 | c.849A>G | synonymous_variant | 1.0 |
rpoB | 760661 | c.855A>C | synonymous_variant | 1.0 |
rpoB | 760670 | c.864G>C | synonymous_variant | 1.0 |
rpoB | 760674 | c.868T>C | synonymous_variant | 1.0 |
rpoB | 760679 | c.873A>G | synonymous_variant | 1.0 |
rpoB | 760683 | c.877T>C | synonymous_variant | 1.0 |
rpoB | 760724 | c.918T>C | synonymous_variant | 1.0 |
rpoB | 760730 | c.924T>C | synonymous_variant | 1.0 |
rpoB | 760748 | c.942C>G | synonymous_variant | 1.0 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.75 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.75 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.67 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.75 |
rpoB | 761266 | p.Asn487Ser | missense_variant | 0.5 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.75 |
rpoB | 761284 | p.Ser493Tyr | missense_variant | 0.5 |
rpoB | 761288 | c.1482G>C | synonymous_variant | 0.5 |
rpoB | 761309 | c.1503C>T | synonymous_variant | 0.5 |
rpoB | 761318 | c.1512G>T | synonymous_variant | 0.75 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.67 |
rpoB | 761516 | c.1710G>C | synonymous_variant | 0.67 |
rpoB | 761522 | c.1716C>T | synonymous_variant | 0.75 |
rpoB | 761528 | c.1722C>T | synonymous_variant | 0.8 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.8 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.86 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.86 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.86 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.86 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 1.0 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 1.0 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 1.0 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 1.0 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 1.0 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 1.0 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 1.0 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 1.0 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 1.0 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 1.0 |
rpoB | 762023 | c.2217C>T | synonymous_variant | 1.0 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 1.0 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 1.0 |
rpoB | 762041 | c.2235C>T | synonymous_variant | 1.0 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 1.0 |
rpoB | 762068 | c.2262C>T | synonymous_variant | 1.0 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 1.0 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
rpoB | 762104 | c.2298C>T | synonymous_variant | 1.0 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 1.0 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 1.0 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
rpoB | 762149 | c.2343G>T | synonymous_variant | 1.0 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 1.0 |
rpoB | 762161 | c.2355C>T | synonymous_variant | 1.0 |
rpoB | 762176 | c.2370T>G | synonymous_variant | 1.0 |
rpoB | 762179 | c.2373C>T | synonymous_variant | 1.0 |
rpoB | 762182 | c.2376C>T | synonymous_variant | 1.0 |
rpoB | 762185 | c.2379G>T | synonymous_variant | 1.0 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 1.0 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
rpoB | 762287 | c.2481C>T | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
rpoB | 762296 | c.2490G>T | synonymous_variant | 1.0 |
rpoB | 762297 | c.2491C>T | synonymous_variant | 1.0 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 1.0 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
rpoB | 762320 | c.2514C>G | synonymous_variant | 1.0 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.67 |
rpoC | 762425 | c.-945C>T | upstream_gene_variant | 0.67 |
rpoB | 762426 | p.Ser874Gln | missense_variant | 0.67 |
rpoC | 762431 | c.-939C>T | upstream_gene_variant | 0.75 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.83 |
rpoC | 762446 | c.-924C>G | upstream_gene_variant | 0.83 |
rpoC | 762449 | c.-921C>T | upstream_gene_variant | 0.83 |
rpoC | 762452 | c.-918G>T | upstream_gene_variant | 0.83 |
rpoC | 762483 | c.-887C>T | upstream_gene_variant | 0.71 |
rpoB | 762489 | p.Val895Lys | missense_variant | 0.67 |
rpoB | 762507 | p.Leu901Met | missense_variant | 0.75 |
rpoB | 762510 | p.Ala902Pro | missense_variant | 0.75 |
rpoC | 762527 | c.-843G>C | upstream_gene_variant | 0.75 |
rpoC | 762866 | c.-504C>T | upstream_gene_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
rpoC | 762890 | c.-480C>T | upstream_gene_variant | 1.0 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.75 |
rpoC | 762920 | c.-450C>G | upstream_gene_variant | 0.75 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.75 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.8 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.8 |
rpoC | 762956 | c.-414G>T | upstream_gene_variant | 0.88 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.88 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.88 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 0.88 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 1.0 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
rpoC | 763041 | c.-329C>T | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 1.0 |
rpoC | 763085 | c.-285C>T | upstream_gene_variant | 1.0 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 1.0 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 1.0 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
rpoC | 763124 | c.-246C>T | upstream_gene_variant | 1.0 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 1.0 |
rpoC | 763145 | c.-225G>A | upstream_gene_variant | 1.0 |
rpoC | 763157 | c.-213G>T | upstream_gene_variant | 1.0 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 1.0 |
rpoC | 763178 | c.-192G>A | upstream_gene_variant | 1.0 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 1.0 |
rpoC | 763196 | c.-174G>A | upstream_gene_variant | 1.0 |
rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
rpoC | 763505 | c.136C>T | synonymous_variant | 1.0 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.67 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.67 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.67 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.67 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.75 |
rpoC | 763570 | c.201G>T | synonymous_variant | 0.67 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.67 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.67 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.67 |
rpoC | 763657 | c.288G>A | synonymous_variant | 0.75 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.67 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.75 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.67 |
rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 0.67 |
rpoC | 763708 | c.339G>T | synonymous_variant | 0.67 |
rpoC | 763711 | c.342G>C | synonymous_variant | 1.0 |
rpoC | 763714 | c.345G>T | synonymous_variant | 1.0 |
rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
rpoC | 763741 | c.372C>T | synonymous_variant | 1.0 |
rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
rpoC | 763765 | c.396T>C | synonymous_variant | 1.0 |
rpoC | 763774 | c.405G>C | synonymous_variant | 1.0 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 1.0 |
rpoC | 763795 | p.Glu142Asp | missense_variant | 1.0 |
rpoC | 763796 | p.Met143Leu | missense_variant | 1.0 |
rpoC | 763807 | c.438T>C | synonymous_variant | 1.0 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 1.0 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 1.0 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 1.0 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 1.0 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 1.0 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.83 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.5 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.67 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.6 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.71 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.71 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.83 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.83 |
rpoC | 764803 | c.1434C>G | synonymous_variant | 0.83 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.83 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.83 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.8 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.8 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
rpoC | 764912 | p.Met515Leu | missense_variant | 1.0 |
rpoC | 764920 | c.1551G>C | synonymous_variant | 1.0 |
rpoC | 764926 | c.1557C>T | synonymous_variant | 1.0 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
rpoC | 764953 | c.1584G>C | synonymous_variant | 1.0 |
rpoC | 764962 | c.1593G>C | synonymous_variant | 1.0 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 1.0 |
rpoC | 765781 | c.2412C>T | synonymous_variant | 1.0 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 1.0 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 1.0 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 1.0 |
rpoC | 765814 | c.2445A>T | synonymous_variant | 1.0 |
rpoC | 765817 | c.2448G>C | synonymous_variant | 1.0 |
rpoC | 765820 | c.2451G>C | synonymous_variant | 1.0 |
rpoC | 765823 | c.2454C>G | synonymous_variant | 1.0 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 1.0 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 1.0 |
rpoC | 765865 | c.2496C>T | synonymous_variant | 1.0 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.5 |
rpoC | 766618 | c.3249G>T | synonymous_variant | 1.0 |
rpoC | 766624 | c.3255G>T | synonymous_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 1.0 |
rpoC | 766660 | c.3291G>T | synonymous_variant | 1.0 |
rpoC | 766661 | p.Val1098Leu | missense_variant | 1.0 |
rpoC | 766667 | p.Ser1100Ala | missense_variant | 0.67 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.67 |
rpoC | 766690 | c.3321G>C | synonymous_variant | 0.5 |
rpoC | 766774 | c.3405T>G | synonymous_variant | 0.5 |
rpoC | 766776 | p.Arg1136His | missense_variant | 0.5 |
rpoC | 766792 | c.3423C>G | synonymous_variant | 0.67 |
rpoC | 766798 | c.3429C>G | synonymous_variant | 0.67 |
rpoC | 766799 | p.Ala1144Ser | missense_variant | 0.67 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.67 |
rpoC | 766813 | c.3444G>C | synonymous_variant | 0.67 |
rpoC | 766837 | c.3468G>C | synonymous_variant | 0.67 |
rpoC | 766945 | c.3576A>C | synonymous_variant | 0.4 |
rpoC | 766948 | c.3579G>C | synonymous_variant | 0.4 |
rpoC | 766951 | c.3582G>C | synonymous_variant | 0.4 |
rpoC | 766960 | c.3591C>T | synonymous_variant | 0.4 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.4 |
rpoC | 766973 | p.Ala1202Ser | missense_variant | 0.6 |
rpoC | 766978 | c.3609C>T | synonymous_variant | 0.6 |
rpoC | 766981 | c.3612T>C | synonymous_variant | 0.6 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.6 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.6 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.6 |
rpsL | 781859 | c.300T>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 | 781880 | c.321C>G | synonymous_variant | 1.0 |
rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
rpsL | 781898 | c.339A>C | synonymous_variant | 1.0 |
rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
rplC | 800610 | c.-199_-197delCTAinsTTG | upstream_gene_variant | 1.0 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 1.0 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 1.0 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 1.0 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 1.0 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 1.0 |
rplC | 800762 | c.-47T>G | upstream_gene_variant | 1.0 |
rrs | 1471914 | n.69A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471943 | n.98T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472089 | n.244C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472222 | n.377G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472229 | n.384C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472497 | n.652G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472518 | n.673G>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472544 | n.699C>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473083 | n.1238G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473089 | n.1244A>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473384 | n.-274A>T | upstream_gene_variant | 0.5 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473758 | n.101G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474350 | n.693G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474527 | n.870T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474528 | n.871T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474530 | n.873G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474542 | n.885A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474552 | n.895C>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474555 | n.898T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474562 | n.905G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474565 | n.908T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474570 | n.913G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474571 | n.914G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474578 | n.921A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474584 | n.927C>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474586 | n.929T>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474638 | n.981C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474664 | n.1007G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474666 | n.1009T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474687 | n.1030C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474711 | n.1054G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474927 | n.1271delC | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474931 | n.1274G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1475049 | n.1392C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475057 | n.1400G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475061 | n.1404C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475076 | n.1419C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475092 | n.1435A>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475094 | n.1437C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475106 | n.1449G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475109 | n.1452C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475115 | n.1458A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475122 | n.1465C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475154 | n.1497C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475167 | n.1510T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475422 | n.1765A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475436 | n.1779C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475555 | n.1898T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475576 | n.1919C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475672 | n.2015C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475687 | n.2030C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475707 | n.2050T>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475735 | n.2078T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475843 | n.2186G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475849 | n.2192G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475853 | n.2196C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.56 |
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 | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476608 | n.2951C>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476621 | n.2964C>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476637 | n.2980C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476657 | n.3000G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 1.0 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 1.0 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 1.0 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 1.0 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.83 |
rpsA | 1833733 | c.192C>T | synonymous_variant | 0.83 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.83 |
rpsA | 1833754 | c.213G>A | synonymous_variant | 0.83 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.83 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 0.67 |
rpsA | 1833770 | p.Asn77Ala | missense_variant | 0.67 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.67 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.67 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.67 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 1.0 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 1.0 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 1.0 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 1.0 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
rpsA | 1833859 | c.318C>G | synonymous_variant | 1.0 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 1.0 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 1.0 |
rpsA | 1833877 | c.336C>G | synonymous_variant | 1.0 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 1.0 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 1.0 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 1.0 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 1.0 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 1.0 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 1.0 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 1.0 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 1.0 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 1.0 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 1.0 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 1.0 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.75 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.75 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.8 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.75 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.75 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.75 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.75 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.75 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.75 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.75 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.75 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.67 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.75 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.75 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.75 |
rpsA | 1834483 | c.942G>A | synonymous_variant | 0.8 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.83 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 1.0 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 1.0 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 1.0 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 1.0 |
rpsA | 1834561 | c.1020C>G | synonymous_variant | 1.0 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
rpsA | 1834627 | c.1086C>G | synonymous_variant | 1.0 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
rpsA | 1834636 | c.1095C>G | synonymous_variant | 1.0 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
rpsA | 1834649 | p.Thr370His | missense_variant | 1.0 |
rpsA | 1834653 | p.Glu371Ala | missense_variant | 1.0 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 1.0 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 1.0 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 1.0 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 1.0 |
katG | 2155691 | c.421T>C | synonymous_variant | 0.67 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.5 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.5 |
katG | 2155728 | c.384G>C | synonymous_variant | 0.5 |
katG | 2155737 | c.375C>T | synonymous_variant | 0.5 |
katG | 2155741 | p.Gly124Ser | missense_variant | 0.5 |
katG | 2155743 | c.369G>A | synonymous_variant | 0.5 |
kasA | 2517917 | c.-198G>C | upstream_gene_variant | 0.5 |
kasA | 2517921 | c.-194_-193delACinsCT | upstream_gene_variant | 0.5 |
kasA | 2517937 | c.-178_-177delGCinsAG | upstream_gene_variant | 0.5 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.5 |
kasA | 2517956 | c.-159G>A | upstream_gene_variant | 0.5 |
rpoA | 3877680 | c.828G>T | synonymous_variant | 0.5 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.5 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.5 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.6 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.6 |
rpoA | 3877731 | c.777G>T | synonymous_variant | 0.6 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.6 |
rpoA | 3877740 | c.768G>C | synonymous_variant | 0.5 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.5 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.5 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.67 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.5 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.5 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.5 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.6 |
rpoA | 3877893 | c.615C>G | synonymous_variant | 0.6 |
rpoA | 3877900 | c.607_608delAGinsTC | synonymous_variant | 0.6 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.6 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.6 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.6 |
rpoA | 3877932 | c.576G>C | synonymous_variant | 0.75 |
rpoA | 3877936 | p.Lys191Arg | missense_variant | 0.75 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.67 |
clpC1 | 4038746 | c.1959C>T | synonymous_variant | 0.67 |
clpC1 | 4038749 | c.1956C>T | synonymous_variant | 0.67 |
clpC1 | 4038755 | c.1950G>T | synonymous_variant | 0.67 |
clpC1 | 4038767 | c.1938G>T | synonymous_variant | 0.75 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.67 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.75 |
clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.8 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.8 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.83 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.8 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.8 |
clpC1 | 4038842 | c.1863G>C | synonymous_variant | 1.0 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.67 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.75 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.8 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.8 |
clpC1 | 4039046 | c.1659C>T | synonymous_variant | 0.8 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 1.0 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 1.0 |
clpC1 | 4039073 | c.1632C>T | synonymous_variant | 1.0 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 1.0 |
clpC1 | 4039082 | c.1623C>T | synonymous_variant | 1.0 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 1.0 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 1.0 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 1.0 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 1.0 |
clpC1 | 4039133 | c.1572C>G | synonymous_variant | 1.0 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 1.0 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 1.0 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 1.0 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 1.0 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 1.0 |
clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 1.0 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.75 |
clpC1 | 4039239 | p.Gly489Ala | missense_variant | 0.75 |
clpC1 | 4039250 | c.1455C>G | synonymous_variant | 0.75 |
clpC1 | 4039427 | p.Glu426Asp | missense_variant | 0.67 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.67 |
clpC1 | 4039436 | c.1269G>A | synonymous_variant | 0.67 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 1.0 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 1.0 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 1.0 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.67 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.67 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.75 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.67 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.5 |
clpC1 | 4039670 | c.1035G>C | synonymous_variant | 0.5 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.5 |
clpC1 | 4039802 | c.903G>C | synonymous_variant | 0.5 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.5 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.5 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.5 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.5 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.5 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.5 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.6 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.75 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.75 |
clpC1 | 4039913 | c.792C>T | synonymous_variant | 0.75 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.67 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.6 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.6 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.6 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.6 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.6 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.6 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.5 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.67 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.75 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.75 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.75 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.67 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 1.0 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 1.0 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 1.0 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
clpC1 | 4040456 | c.249C>G | synonymous_variant | 1.0 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
clpC1 | 4040468 | c.237G>C | synonymous_variant | 1.0 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
clpC1 | 4040477 | c.228G>T | synonymous_variant | 0.67 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
clpC1 | 4040501 | c.204C>G | synonymous_variant | 1.0 |
clpC1 | 4040516 | c.189C>G | synonymous_variant | 1.0 |