Linked Data
ClinVar Variation Id:
283451
dbSNP Id:
rs886042627
gnomAD v2:
9-134386736-C-T
gnomAD v3:
9-131511349-C-T
gnomAD v4:
9-131511349-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131511349C>T , CM000671.2:g.131511349C>T | GRCh38 |
| NC_000009.11:g.134386736C>T , CM000671.1:g.134386736C>T | GRCh37 |
| NC_000009.10:g.133376557C>T | NCBI36 |
| NG_008896.1:g.13448C>T | |
| NG_008896.2:g.13448C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.706C>T | ENSP00000343034.7:p.Arg236Trp | |
| ENST00000404875.7:n.1240C>T | ||
| ENST00000423007.6:c.925C>T | ENSP00000404119.2:p.Arg309Trp | |
| ENST00000677295.2:c.*1207C>T | ENSP00000504346.2:n.*1207C>T | |
| ENST00000678264.2:c.*1051C>T | ENSP00000503157.2:n.*1051C>T | |
| ENST00000678942.2:c.*421C>T | ENSP00000504690.2:n.*421C>T | |
| ENST00000682070.1:n.1328C>T | ||
| ENST00000682813.1:n.1133C>T | ||
| ENST00000683134.1:c.235C>T | ||
| ENST00000683392.1:n.3615C>T | ||
| ENST00000683712.1:n.1268C>T | ||
| ENST00000683900.1:n.2195C>T | ||
| ENST00000684062.1:n.1534C>T | ||
| ENST00000684579.1:n.2709C>T | ||
| ENST00000341012.12:c.706C>T | ENSP00000343034.7:p.Arg236Trp | |
| ENST00000372220.5:c.-145-692C>T | ENSP00000361294.5:n.-145-692C>T | |
| ENST00000372228.9:c.934C>T | ENSP00000361302.3:p.Arg312Trp | |
| ENST00000402686.8:c.868C>T MANE Select | ENSP00000385797.4:p.Arg290Trp | |
| ENST00000415075.6:c.*321C>T | ENSP00000405149.2:n.*321C>T | |
| ENST00000676640.1:c.868C>T | ENSP00000503281.1:p.Arg290Trp | |
| ENST00000676803.1:c.43C>T | ENSP00000503093.1:p.Arg15Trp | |
| ENST00000676835.1:c.*78C>T | ENSP00000502911.1:n.*78C>T | |
| ENST00000677029.1:c.412C>T | ENSP00000502936.1:p.Arg138Trp | |
| ENST00000677099.1:c.*578C>T | ENSP00000504553.1:n.*578C>T | |
| ENST00000677216.1:c.517C>T | ENSP00000503772.1:p.Arg173Trp | |
| ENST00000677293.1:c.43C>T | ENSP00000504278.1:p.Arg15Trp | |
| ENST00000677295.1:c.*240C>T | ENSP00000504346.1:n.*240C>T | |
| ENST00000677444.1:c.674C>T | ||
| ENST00000677586.1:n.349C>T | ||
| ENST00000677626.1:c.706C>T | ENSP00000503552.1:p.Arg236Trp | |
| ENST00000677677.1:n.828C>T | ||
| ENST00000677853.1:c.449C>T | ENSP00000503488.1:p.Ser150Leu | |
| ENST00000677944.1:c.130C>T | ||
| ENST00000678264.1:c.*240C>T | ENSP00000503157.1:n.*240C>T | |
| ENST00000678303.1:c.778C>T | ENSP00000503696.1:p.Arg260Trp | |
| ENST00000678366.1:c.*1117C>T | ENSP00000504353.1:n.*1117C>T | |
| ENST00000678546.1:c.*240C>T | ENSP00000503062.1:n.*240C>T | |
| ENST00000678548.1:c.*935C>T | ENSP00000503934.1:n.*935C>T | |
| ENST00000678626.1:n.560C>T | ||
| ENST00000678707.1:n.506C>T | ||
| ENST00000678733.1:c.42C>T | ||
| ENST00000678739.1:c.*1189C>T | ENSP00000503806.1:n.*1189C>T | |
| ENST00000678833.1:c.*315C>T | ENSP00000503893.1:n.*315C>T | |
| ENST00000678942.1:c.43C>T | ENSP00000504690.1:p.Arg15Trp | |
| ENST00000679023.1:c.706C>T | ENSP00000503718.1:p.Arg236Trp | |
| ENST00000679073.1:c.246C>T | ENSP00000504356.1:n.246C>T | |
| ENST00000679076.1:c.482C>T | ||
| ENST00000679111.1:c.868C>T | ENSP00000504257.1:p.Arg290Trp | |
| ENST00000679189.1:c.517C>T | ENSP00000503356.1:p.Arg173Trp | |
| ENST00000341012.11:c.706C>T | ENSP00000343034.7:p.Arg236Trp | |
| ENST00000372228.7:c.934C>T | ENSP00000361302.3:p.Arg312Trp | |
| ENST00000402686.7:c.868C>T | ENSP00000385797.3:p.Arg290Trp | |
| ENST00000404875.6:c.517C>T | ENSP00000384531.2:p.Arg173Trp | |
| ENST00000415075.5:c.260C>T | ENSP00000405149.1:p.Ser87Leu | |
| ENST00000423007.5:c.868C>T | ENSP00000404119.1:p.Arg290Trp | |
| ENST00000441334.5:c.583C>T | ENSP00000395060.1:p.Arg195Trp | |
| ENST00000462375.5:n.689C>T | ||
| ENST00000485278.5:n.850C>T | ||
| NM_001077365.1:c.868C>T | NP_001070833.1:p.Arg290Trp | |
| NM_001077366.1:c.706C>T | NP_001070834.1:p.Arg236Trp | |
| NM_001136113.1:c.868C>T | NP_001129585.1:p.Arg290Trp | |
| NM_001136114.1:c.517C>T | NP_001129586.1:p.Arg173Trp | |
| NM_007171.3:c.934C>T | NP_009102.3:p.Arg312Trp | |
| XM_005272156.1:c.934C>T | XP_005272213.1:p.Arg312Trp | |
| XM_005272158.1:c.772C>T | XP_005272215.1:p.Arg258Trp | |
| XM_005272159.1:c.583C>T | XP_005272216.1:p.Arg195Trp | |
| XM_005272162.1:c.-269C>T | XP_005272219.1:n.-269C>T | |
| XM_006716932.1:c.583C>T | XP_006716995.1:p.Arg195Trp | |
| XM_011518140.1:c.787C>T | XP_011516442.1:p.Arg263Trp | |
| XM_011518141.1:c.721C>T | XP_011516443.1:p.Arg241Trp | |
| XM_011518142.1:c.625C>T | XP_011516444.1:p.Arg209Trp | |
| XM_011518143.1:c.614C>T | XP_011516445.1:p.Ser205Leu | |
| XM_011518144.1:c.934C>T | XP_011516446.1:p.Arg312Trp | |
| XM_011518145.1:c.478C>T | XP_011516447.1:p.Arg160Trp | |
| XM_011518146.1:c.614C>T | XP_011516448.1:p.Ser205Leu | |
| XR_929703.1:n.1110C>T | ||
| NM_001353193.1:c.934C>T | NP_001340122.1:p.Arg312Trp | |
| NM_001353194.1:c.706C>T | NP_001340123.1:p.Arg236Trp | |
| NM_001353195.1:c.517C>T | NP_001340124.1:p.Arg173Trp | |
| NM_001353196.1:c.778C>T | NP_001340125.1:p.Arg260Trp | |
| NM_001353197.1:c.772C>T | NP_001340126.1:p.Arg258Trp | |
| NM_001353198.1:c.772C>T | NP_001340127.1:p.Arg258Trp | |
| NM_001353199.1:c.583C>T | NP_001340128.1:p.Arg195Trp | |
| NM_001353200.1:c.412C>T | NP_001340129.1:p.Arg138Trp | |
| NR_148391.1:n.918C>T | ||
| NR_148392.1:n.1136C>T | ||
| NR_148393.1:n.918C>T | ||
| NR_148394.1:n.806C>T | ||
| NR_148395.1:n.1070C>T | ||
| NR_148396.1:n.699C>T | ||
| NR_148397.1:n.963C>T | ||
| NR_148398.1:n.918C>T | ||
| NR_148399.1:n.1310C>T | ||
| NR_148400.1:n.904C>T | ||
| XM_005272162.3:c.-269C>T | XP_005272219.1:n.-269C>T | |
| XM_006716932.2:c.583C>T | XP_006716995.1:p.Arg195Trp | |
| XM_011518140.2:c.787C>T | XP_011516442.1:p.Arg263Trp | |
| XM_011518141.2:c.721C>T | XP_011516443.1:p.Arg241Trp | |
| XM_011518142.2:c.625C>T | XP_011516444.1:p.Arg209Trp | |
| XM_011518143.2:c.614C>T | XP_011516445.1:p.Ser205Leu | |
| XM_011518145.2:c.478C>T | XP_011516447.1:p.Arg160Trp | |
| XM_017014205.2:c.-269C>T | XP_016869694.1:n.-269C>T | |
| XM_024447380.1:c.-269C>T | XP_024303148.1:n.-269C>T | |
| XM_024447381.1:c.43C>T | XP_024303149.1:p.Arg15Trp | |
| XM_024447382.1:c.-269C>T | XP_024303150.1:n.-269C>T | |
| XR_001746160.2:n.1038C>T | ||
| XR_001746162.2:n.1104C>T | ||
| XR_001746164.1:n.816C>T | ||
| XR_001746166.2:n.1255C>T | ||
| NM_001077365.2:c.868C>T MANE Select | NP_001070833.1:p.Arg290Trp | |
| NM_001077366.2:c.706C>T | NP_001070834.1:p.Arg236Trp | |
| NM_001136113.2:c.868C>T | NP_001129585.1:p.Arg290Trp | |
| NM_001136114.2:c.517C>T | NP_001129586.1:p.Arg173Trp | |
| NM_001353193.2:c.934C>T | NP_001340122.2:p.Arg312Trp | |
| NM_001353194.2:c.706C>T | NP_001340123.1:p.Arg236Trp | |
| NM_001353195.2:c.517C>T | NP_001340124.1:p.Arg173Trp | |
| NM_001353196.2:c.778C>T | NP_001340125.1:p.Arg260Trp | |
| NM_001353197.2:c.772C>T | NP_001340126.2:p.Arg258Trp | |
| NM_001353198.2:c.772C>T | NP_001340127.2:p.Arg258Trp | |
| NM_001353199.2:c.583C>T | NP_001340128.2:p.Arg195Trp | |
| NM_001353200.2:c.412C>T | NP_001340129.1:p.Arg138Trp | |
| NM_001374689.1:c.851C>T | NP_001361618.1:p.Ser284Leu | |
| NM_001374690.1:c.868C>T | NP_001361619.1:p.Arg290Trp | |
| NM_001374691.1:c.517C>T | NP_001361620.1:p.Arg173Trp | |
| NM_001374692.1:c.517C>T | NP_001361621.1:p.Arg173Trp | |
| NM_001374693.1:c.706C>T | NP_001361622.1:p.Arg236Trp | |
| NM_001374695.1:c.478C>T | NP_001361624.1:p.Arg160Trp | |
| NM_007171.4:c.934C>T | NP_009102.4:p.Arg312Trp | |
| NR_148391.2:n.902C>T | ||
| NR_148392.2:n.1120C>T | ||
| NR_148393.2:n.902C>T | ||
| NR_148394.2:n.790C>T | ||
| NR_148395.2:n.1054C>T | ||
| NR_148396.2:n.683C>T | ||
| NR_148397.2:n.947C>T | ||
| NR_148398.2:n.902C>T | ||
| NR_148399.2:n.1294C>T | ||
| NR_148400.2:n.888C>T |