ClinVar RCV:
ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00008862 (EAS)
Exomes Max Group AF
0.00008231 (EAS)
Revel Score:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.49110273G>A , CM000665.2:g.49110273G>A | GRCh38 |
| NC_000003.11:g.49147706G>A , CM000665.1:g.49147706G>A | GRCh37 |
| NC_000003.10:g.49122710G>A | NCBI36 |
| NG_054716.1:g.15666C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698200.1:c.3730C>T | ENSP00000513604.2:p.Arg1244Trp | |
| ENST00000306026.6:c.3904C>T | ENSP00000303503.6:p.Arg1302Trp | |
| ENST00000398896.6:c.3601C>T | ENSP00000381870.3:p.Arg1201Trp | |
| ENST00000417901.6:c.3949C>T MANE Select | ENSP00000395260.1:p.Arg1317Trp | |
| ENST00000689715.1:c.3793C>T | ENSP00000510256.1:p.Arg1265Trp | |
| ENST00000691288.1:c.3607C>T | ENSP00000508481.1:p.Arg1203Trp | |
| ENST00000692912.1:c.3949C>T | ENSP00000508993.1:p.Arg1317Trp | |
| ENST00000693111.1:c.*60C>T | ENSP00000509474.1:n.*60C>T | |
| ENST00000398888.6:c.3640C>T | ENSP00000381863.2:p.Arg1214Trp | |
| ENST00000398892.7:c.3760C>T | ENSP00000381867.3:p.Arg1254Trp | |
| ENST00000398896.5:c.3335C>T | ||
| ENST00000398898.6:c.3760C>T | ENSP00000381872.2:p.Arg1254Trp | |
| ENST00000417901.5:c.3949C>T | ENSP00000395260.1:p.Arg1317Trp | |
| ENST00000434032.6:c.3943C>T | ENSP00000401197.2:p.Arg1315Trp | |
| ENST00000453664.5:c.3913C>T | ENSP00000400090.1:p.Arg1305Trp | |
| ENST00000483667.1:n.298C>T | ||
| NM_001199160.1:c.3943C>T | NP_001186089.1:p.Arg1315Trp | |
| NM_001199161.1:c.3949C>T | NP_001186090.1:p.Arg1317Trp | |
| NM_001199162.1:c.3913C>T | NP_001186091.1:p.Arg1305Trp | |
| NM_006677.2:c.3640C>T | NP_006668.1:p.Arg1214Trp | |
| XM_005264823.1:c.3955C>T | XP_005264880.1:p.Arg1319Trp | |
| XM_005264824.2:c.3955C>T | XP_005264881.1:p.Arg1319Trp | |
| XM_005264825.1:c.3949C>T | XP_005264882.1:p.Arg1317Trp | |
| XM_005264826.1:c.3949C>T | XP_005264883.1:p.Arg1317Trp | |
| XM_005264827.1:c.3910C>T | XP_005264884.1:p.Arg1304Trp | |
| XM_005264829.1:c.3955C>T | XP_005264886.1:p.Arg1319Trp | |
| XM_005264830.1:c.3652C>T | XP_005264887.1:p.Arg1218Trp | |
| XM_005264831.1:c.3601C>T | XP_005264888.1:p.Arg1201Trp | |
| XM_006712946.1:c.3952C>T | XP_006713009.1:p.Arg1318Trp | |
| XM_006712947.1:c.3901C>T | XP_006713010.1:p.Arg1301Trp | |
| XM_006712948.1:c.3943C>T | XP_006713011.1:p.Arg1315Trp | |
| XM_006712949.1:c.3805C>T | XP_006713012.1:p.Arg1269Trp | |
| XM_006712950.1:c.3904C>T | XP_006713013.1:p.Arg1302Trp | |
| XM_006712951.1:c.3901C>T | XP_006713014.1:p.Arg1301Trp | |
| XM_006712952.1:c.3898C>T | XP_006713015.1:p.Arg1300Trp | |
| XM_006712953.1:c.3898C>T | XP_006713016.1:p.Arg1300Trp | |
| NM_001351098.1:c.3910C>T | NP_001338027.1:p.Arg1304Trp | |
| NM_001351099.1:c.3940C>T | NP_001338028.1:p.Arg1314Trp | |
| NM_001351100.1:c.3946C>T | NP_001338029.1:p.Arg1316Trp | |
| NM_001351101.1:c.3949C>T | NP_001338030.1:p.Arg1317Trp | |
| NM_001351102.1:c.3601C>T | NP_001338031.1:p.Arg1201Trp | |
| NM_001351103.1:c.3646C>T | NP_001338032.1:p.Arg1216Trp | |
| NM_001351104.1:c.3652C>T | NP_001338033.1:p.Arg1218Trp | |
| NM_001351105.1:c.3793C>T | NP_001338034.1:p.Arg1265Trp | |
| NM_001351106.1:c.3646C>T | NP_001338035.1:p.Arg1216Trp | |
| NM_001351107.1:c.3904C>T | NP_001338036.1:p.Arg1302Trp | |
| NM_001351108.1:c.3607C>T | NP_001338037.1:p.Arg1203Trp | |
| XM_005264823.3:c.3955C>T | XP_005264880.1:p.Arg1319Trp | |
| XM_005264825.3:c.3949C>T | XP_005264882.1:p.Arg1317Trp | |
| XM_005264826.3:c.3949C>T | XP_005264883.1:p.Arg1317Trp | |
| XM_005264827.2:c.3910C>T | XP_005264884.1:p.Arg1304Trp | |
| XM_005264829.3:c.3955C>T | XP_005264886.1:p.Arg1319Trp | |
| XM_005264830.3:c.3652C>T | XP_005264887.1:p.Arg1218Trp | |
| XM_006712946.3:c.3952C>T | XP_006713009.1:p.Arg1318Trp | |
| XM_006712947.2:c.3901C>T | XP_006713010.1:p.Arg1301Trp | |
| XM_006712948.3:c.3943C>T | XP_006713011.1:p.Arg1315Trp | |
| XM_006712949.3:c.3805C>T | XP_006713012.1:p.Arg1269Trp | |
| XM_006712951.2:c.3901C>T | XP_006713014.1:p.Arg1301Trp | |
| XM_006712952.2:c.3898C>T | XP_006713015.1:p.Arg1300Trp | |
| XM_017005616.2:c.3940C>T | XP_016861105.1:p.Arg1314Trp | |
| XM_017005617.1:c.3904C>T | XP_016861106.1:p.Arg1302Trp | |
| XM_017005619.2:c.3946C>T | XP_016861108.1:p.Arg1316Trp | |
| XM_017005621.2:c.3799C>T | XP_016861110.1:p.Arg1267Trp | |
| XM_017005624.2:c.3793C>T | XP_016861113.1:p.Arg1265Trp | |
| XM_017005625.2:c.3646C>T | XP_016861114.1:p.Arg1216Trp | |
| XM_017005626.1:c.3640C>T | XP_016861115.1:p.Arg1214Trp | |
| XM_017005627.1:c.3607C>T | XP_016861116.1:p.Arg1203Trp | |
| XM_017005628.1:c.3601C>T | XP_016861117.1:p.Arg1201Trp | |
| XM_017005629.1:c.3595C>T | XP_016861118.1:p.Arg1199Trp | |
| XM_017005633.2:c.3640C>T | XP_016861122.1:p.Arg1214Trp | |
| XM_017005635.1:c.2299C>T | XP_016861124.1:p.Arg767Trp | |
| NM_001199160.2:c.3943C>T | NP_001186089.1:p.Arg1315Trp | |
| NM_001199161.2:c.3949C>T MANE Select | NP_001186090.1:p.Arg1317Trp | |
| NM_001199162.2:c.3913C>T | NP_001186091.1:p.Arg1305Trp | |
| NM_001351098.2:c.3910C>T | NP_001338027.1:p.Arg1304Trp | |
| NM_001351099.2:c.3940C>T | NP_001338028.1:p.Arg1314Trp | |
| NM_001351100.2:c.3946C>T | NP_001338029.1:p.Arg1316Trp | |
| NM_001351101.2:c.3949C>T | NP_001338030.1:p.Arg1317Trp | |
| NM_001351102.2:c.3601C>T | NP_001338031.1:p.Arg1201Trp | |
| NM_001351103.2:c.3646C>T | NP_001338032.1:p.Arg1216Trp | |
| NM_001351104.2:c.3652C>T | NP_001338033.1:p.Arg1218Trp | |
| NM_001351105.2:c.3793C>T | NP_001338034.1:p.Arg1265Trp | |
| NM_001351106.2:c.3646C>T | NP_001338035.1:p.Arg1216Trp | |
| NM_001351107.2:c.3904C>T | NP_001338036.1:p.Arg1302Trp | |
| NM_001351108.2:c.3607C>T | NP_001338037.1:p.Arg1203Trp | |
| NM_001389594.1:c.3949C>T | NP_001376523.1:p.Arg1317Trp | |
| NM_001389595.1:c.3949C>T | NP_001376524.1:p.Arg1317Trp | |
| NM_001389596.1:c.3955C>T | NP_001376525.1:p.Arg1319Trp | |
| NM_001389597.1:c.3652C>T | NP_001376526.1:p.Arg1218Trp | |
| NM_001389598.1:c.3943C>T | NP_001376527.1:p.Arg1315Trp | |
| NM_001389599.1:c.3901C>T | NP_001376528.1:p.Arg1301Trp | |
| NM_001389600.1:c.3898C>T | NP_001376529.1:p.Arg1300Trp | |
| NM_001389601.1:c.3898C>T | NP_001376530.1:p.Arg1300Trp | |
| NM_001389602.1:c.3940C>T | NP_001376531.1:p.Arg1314Trp | |
| NM_001389603.1:c.3904C>T | NP_001376532.1:p.Arg1302Trp | |
| NM_001389604.1:c.3946C>T | NP_001376533.1:p.Arg1316Trp | |
| NM_001389605.1:c.3793C>T | NP_001376534.1:p.Arg1265Trp | |
| NM_001389606.1:c.3646C>T | NP_001376535.1:p.Arg1216Trp | |
| NM_001389607.1:c.3601C>T | NP_001376536.1:p.Arg1201Trp | |
| NM_001389608.1:c.3640C>T | NP_001376537.1:p.Arg1214Trp | |
| NM_006677.3:c.3640C>T | NP_006668.1:p.Arg1214Trp | |
| NM_001400288.1:c.3949C>T | NP_001387217.1:p.Arg1317Trp | |
| NM_001400290.1:c.3952C>T | NP_001387219.1:p.Arg1318Trp | |
| NM_001400292.1:c.3949C>T | NP_001387221.1:p.Arg1317Trp | |
| NM_001400293.1:c.3943C>T | NP_001387222.1:p.Arg1315Trp | |
| NM_001400294.1:c.3934C>T | NP_001387223.1:p.Arg1312Trp | |
| NM_001400295.1:c.3907C>T | NP_001387224.1:p.Arg1303Trp | |
| NM_001400296.1:c.3904C>T | NP_001387225.1:p.Arg1302Trp | |
| NM_001400297.1:c.3904C>T | NP_001387226.1:p.Arg1302Trp | |
| NM_001400298.1:c.3895C>T | NP_001387227.1:p.Arg1299Trp | |
| NM_001400299.1:c.3874C>T | NP_001387228.1:p.Arg1292Trp |