ClinVar Miner

List of variants in gene RAF1 reported as uncertain significance for Cardiovascular phenotype

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Total variants: 118
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HGVS dbSNP gnomAD frequency
NM_002880.4(RAF1):c.94A>G (p.Ile32Val) rs372738063 0.00013
NM_002880.4(RAF1):c.1721A>G (p.Tyr574Cys) rs370242565 0.00012
NM_002880.4(RAF1):c.365T>C (p.Ile122Thr) rs730881000 0.00007
NM_002880.4(RAF1):c.1814C>T (p.Ser605Phe) rs730881004 0.00006
NM_002880.4(RAF1):c.1663G>C (p.Asp555His) rs371704292 0.00004
NM_002880.4(RAF1):c.1913C>T (p.Thr638Met) rs730881007 0.00004
NM_002880.4(RAF1):c.1879C>T (p.Arg627Trp) rs730881005 0.00003
NM_002880.4(RAF1):c.428G>A (p.Arg143Gln) rs750697353 0.00003
NM_002880.4(RAF1):c.293T>C (p.Val98Ala) rs763559779 0.00002
NM_002880.4(RAF1):c.793A>G (p.Met265Val) rs533494009 0.00002
NM_002880.4(RAF1):c.819C>G (p.Asp273Glu) rs771675427 0.00002
NM_002880.4(RAF1):c.917C>T (p.Ser306Leu) rs886041231 0.00002
NM_002880.4(RAF1):c.-4A>C rs368465923 0.00001
NM_002880.4(RAF1):c.1050G>T (p.Met350Ile) rs368860450 0.00001
NM_002880.4(RAF1):c.1247A>G (p.Asn416Ser) rs774198365 0.00001
NM_002880.4(RAF1):c.1334T>G (p.Leu445Arg) rs757591797 0.00001
NM_002880.4(RAF1):c.1553G>A (p.Arg518Gln) rs149580968 0.00001
NM_002880.4(RAF1):c.1657A>C (p.Asn553His) rs745876012 0.00001
NM_002880.4(RAF1):c.1741A>G (p.Met581Val) rs752063874 0.00001
NM_002880.4(RAF1):c.1885G>T (p.Ala629Ser) rs1243841152 0.00001
NM_002880.4(RAF1):c.1901T>C (p.Ile634Thr) rs1013186582 0.00001
NM_002880.4(RAF1):c.1910G>A (p.Cys637Tyr) rs769639669 0.00001
NM_002880.4(RAF1):c.23G>C (p.Trp8Ser) rs780550449 0.00001
NM_002880.4(RAF1):c.31A>T (p.Ile11Phe) rs779001930 0.00001
NM_002880.4(RAF1):c.347C>G (p.Thr116Ser) rs1285131074 0.00001
NM_002880.4(RAF1):c.462C>G (p.Ile154Met) rs367732360 0.00001
NM_002880.4(RAF1):c.482A>G (p.Asn161Ser) rs775781057 0.00001
NM_002880.4(RAF1):c.589C>G (p.Pro197Ala) rs563575013 0.00001
NM_002880.4(RAF1):c.676G>A (p.Val226Ile) rs746448519 0.00001
NM_002880.4(RAF1):c.683C>G (p.Ser228Cys) rs766437069 0.00001
NM_002880.4(RAF1):c.770C>G (p.Ser257Trp) rs80338796 0.00001
NM_002880.4(RAF1):c.791A>T (p.His264Leu) rs1057517887 0.00001
NM_002880.4(RAF1):c.835G>A (p.Asp279Asn) rs368796800 0.00001
NM_002880.4(RAF1):c.845G>A (p.Arg282Gln) rs752713997 0.00001
NM_002880.4(RAF1):c.915G>T (p.Trp305Cys) rs774670909 0.00001
NM_002880.4(RAF1):c.953G>A (p.Arg318Gln) rs757937109 0.00001
NM_002880.3(RAF1):c.1109_1111delGAG
NM_002880.4(RAF1):c.1019A>G (p.Tyr340Cys) rs2058798881
NM_002880.4(RAF1):c.113A>C (p.Tyr38Ser) rs576041742
NM_002880.4(RAF1):c.1148C>A (p.Thr383Asn)
NM_002880.4(RAF1):c.1156C>G (p.Gln386Glu)
NM_002880.4(RAF1):c.1178A>C (p.Glu393Ala) rs886042569
NM_002880.4(RAF1):c.1271G>A (p.Cys424Tyr)
NM_002880.4(RAF1):c.1301A>G (p.His434Arg)
NM_002880.4(RAF1):c.1324A>G (p.Met442Val)
NM_002880.4(RAF1):c.1342A>G (p.Ile448Val)
NM_002880.4(RAF1):c.1415A>G (p.Asn472Ser)
NM_002880.4(RAF1):c.142C>G (p.Leu48Val) rs752967378
NM_002880.4(RAF1):c.1442C>T (p.Thr481Ile)
NM_002880.4(RAF1):c.1483C>T (p.Arg495Cys)
NM_002880.4(RAF1):c.1496C>G (p.Ser499Cys)
NM_002880.4(RAF1):c.1564AAC[1] (p.Asn523del)
NM_002880.4(RAF1):c.1564_1566delinsGAT (p.Asn522Asp)
NM_002880.4(RAF1):c.1566C>G (p.Asn522Lys)
NM_002880.4(RAF1):c.1606A>G (p.Ile536Val)
NM_002880.4(RAF1):c.1613T>C (p.Leu538Ser) rs730881011
NM_002880.4(RAF1):c.1636C>A (p.Leu546Ile) rs1265418262
NM_002880.4(RAF1):c.1655A>G (p.Asn552Ser) rs775817988
NM_002880.4(RAF1):c.1656C>G (p.Asn552Lys)
NM_002880.4(RAF1):c.1657A>G (p.Asn553Asp)
NM_002880.4(RAF1):c.1661G>A (p.Arg554Gln)
NM_002880.4(RAF1):c.1668+5G>A
NM_002880.4(RAF1):c.1690G>A (p.Gly564Arg) rs1553609909
NM_002880.4(RAF1):c.1696G>A (p.Ala566Thr) rs750077934
NM_002880.4(RAF1):c.169A>G (p.Thr57Ala)
NM_002880.4(RAF1):c.16G>A (p.Gly6Arg) rs1575600689
NM_002880.4(RAF1):c.1748G>C (p.Arg583Thr)
NM_002880.4(RAF1):c.1802A>G (p.Gln601Arg) rs1398402832
NM_002880.4(RAF1):c.1811C>G (p.Ser604Cys)
NM_002880.4(RAF1):c.1850A>T (p.Asn617Ile)
NM_002880.4(RAF1):c.1853G>A (p.Arg618Gln)
NM_002880.4(RAF1):c.1864G>A (p.Glu622Lys)
NM_002880.4(RAF1):c.1880G>C (p.Arg627Pro)
NM_002880.4(RAF1):c.188C>T (p.Pro63Leu)
NM_002880.4(RAF1):c.1896G>C (p.Glu632Asp)
NM_002880.4(RAF1):c.1907C>T (p.Ala636Val)
NM_002880.4(RAF1):c.1912A>T (p.Thr638Ser)
NM_002880.4(RAF1):c.218G>A (p.Arg73Gln) rs140884322
NM_002880.4(RAF1):c.305_307del (p.Leu102del)
NM_002880.4(RAF1):c.309C>G (p.His103Gln) rs1057520880
NM_002880.4(RAF1):c.310G>C (p.Glu104Gln)
NM_002880.4(RAF1):c.332G>A (p.Arg111His) rs996417348
NM_002880.4(RAF1):c.356C>T (p.Ala119Val) rs1398525119
NM_002880.4(RAF1):c.377T>C (p.Leu126Pro)
NM_002880.4(RAF1):c.37A>G (p.Asn13Asp)
NM_002880.4(RAF1):c.38A>G (p.Asn13Ser)
NM_002880.4(RAF1):c.400G>T (p.Val134Phe)
NM_002880.4(RAF1):c.412A>G (p.Thr138Ala)
NM_002880.4(RAF1):c.418A>G (p.Asn140Asp)
NM_002880.4(RAF1):c.419A>G (p.Asn140Ser) rs876657968
NM_002880.4(RAF1):c.440T>C (p.Leu147Pro)
NM_002880.4(RAF1):c.444G>C (p.Lys148Asn) rs1553614733
NM_002880.4(RAF1):c.448G>A (p.Ala150Thr)
NM_002880.4(RAF1):c.577C>T (p.Leu193Phe)
NM_002880.4(RAF1):c.580T>A (p.Leu194Ile)
NM_002880.4(RAF1):c.602T>C (p.Ile201Thr) rs369852728
NM_002880.4(RAF1):c.629C>T (p.Pro210Leu)
NM_002880.4(RAF1):c.641T>C (p.Met214Thr)
NM_002880.4(RAF1):c.644G>A (p.Arg215His)
NM_002880.4(RAF1):c.647G>A (p.Arg216His) rs761703202
NM_002880.4(RAF1):c.65T>G (p.Phe22Cys) rs2125453485
NM_002880.4(RAF1):c.672G>T (p.Met224Ile) rs1553614191
NM_002880.4(RAF1):c.68A>G (p.Asp23Gly)
NM_002880.4(RAF1):c.695A>G (p.Tyr232Cys)
NM_002880.4(RAF1):c.716C>T (p.Thr239Ile)
NM_002880.4(RAF1):c.739T>C (p.Ser247Pro)
NM_002880.4(RAF1):c.752T>A (p.Leu251His) rs1553613787
NM_002880.4(RAF1):c.784A>C (p.Asn262His) rs1575573204
NM_002880.4(RAF1):c.784A>T (p.Asn262Tyr) rs1575573204
NM_002880.4(RAF1):c.834+4A>C rs2058950056
NM_002880.4(RAF1):c.848G>C (p.Ser283Thr)
NM_002880.4(RAF1):c.868_870delinsACC (p.Pro290Thr) rs2125380943
NM_002880.4(RAF1):c.887G>T (p.Ser296Ile) rs762326811
NM_002880.4(RAF1):c.91A>G (p.Thr31Ala) rs1486365900
NM_002880.4(RAF1):c.930_941del (p.Pro311_Ala314del)
NM_002880.4(RAF1):c.934G>T (p.Val312Leu)
NM_002880.4(RAF1):c.97G>A (p.Val33Ile) rs1575600440
NM_002880.4(RAF1):c.988A>G (p.Ile330Val)

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