ClinVar Miner

List of variants in gene RAF1 reported as uncertain significance for not specified

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Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_002880.4(RAF1):c.-209G>A rs727504351 0.00035
NM_002880.4(RAF1):c.212A>G (p.Asn71Ser) rs184022679 0.00029
NM_002880.4(RAF1):c.1721A>G (p.Tyr574Cys) rs370242565 0.00012
NM_002880.4(RAF1):c.1537-13G>A rs369039413 0.00011
NM_002880.4(RAF1):c.935T>C (p.Val312Ala) rs370243307 0.00010
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.1109-17G>C rs770431112 0.00003
NM_002880.4(RAF1):c.1921A>G (p.Thr641Ala) rs1183812590 0.00003
NM_002880.3(RAF1):c.-361G>T rs727504376 0.00002
NM_002880.4(RAF1):c.1193+17C>T rs753928357 0.00002
NM_002880.4(RAF1):c.313C>G (p.His105Asp) rs397516818 0.00002
NM_002880.4(RAF1):c.819C>G (p.Asp273Glu) rs771675427 0.00002
NM_002880.4(RAF1):c.952C>T (p.Arg318Trp) rs759433668 0.00002
NM_002880.4(RAF1):c.-4A>C rs368465923 0.00001
NM_002880.4(RAF1):c.1063A>G (p.Ile355Val) rs727504719 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.1355C>T (p.Thr452Met) rs555781462 0.00001
NM_002880.4(RAF1):c.1688G>A (p.Arg563Gln) rs727504827 0.00001
NM_002880.4(RAF1):c.1741A>G (p.Met581Val) rs752063874 0.00001
NM_002880.4(RAF1):c.1895_1918del (p.Glu632_Thr640delinsAla) rs2058255431 0.00001
NM_002880.4(RAF1):c.1910G>A (p.Cys637Tyr) rs769639669 0.00001
NM_002880.4(RAF1):c.1928C>T (p.Pro643Leu) rs1382398408 0.00001
NM_002880.4(RAF1):c.321T>C (p.Gly107=) rs201937982 0.00001
NM_002880.4(RAF1):c.331C>T (p.Arg111Cys) rs773801570 0.00001
NM_002880.4(RAF1):c.424-6T>C rs983999914 0.00001
NM_002880.4(RAF1):c.482A>G (p.Asn161Ser) rs775781057 0.00001
NM_002880.4(RAF1):c.536A>G (p.Lys179Arg) rs1271531726 0.00001
NM_002880.4(RAF1):c.845G>A (p.Arg282Gln) rs752713997 0.00001
NM_002880.4(RAF1):c.974A>C (p.Gln325Pro) rs764719098 0.00001
NM_002880.3(RAF1):c.(?_-26)-50_(1370_?)+72dup
NM_002880.3(RAF1):c.1804-11_1804-7dup rs727503382
NM_002880.4(RAF1):c.-40C>T rs727503385
NM_002880.4(RAF1):c.1016G>A (p.Ser339Asn) rs1057518084
NM_002880.4(RAF1):c.1144C>T (p.Pro382Ser) rs1575546471
NM_002880.4(RAF1):c.1193+13C>T
NM_002880.4(RAF1):c.1194-17TCCCC[2] rs2058496555
NM_002880.4(RAF1):c.124_125delinsAT (p.Ala42Ile) rs876657965
NM_002880.4(RAF1):c.1483C>T (p.Arg495Cys)
NM_002880.4(RAF1):c.1528C>T (p.Leu510Phe) rs397516816
NM_002880.4(RAF1):c.1613T>C (p.Leu538Ser) rs730881011
NM_002880.4(RAF1):c.1673T>C (p.Ile558Thr) rs1559399152
NM_002880.4(RAF1):c.1708C>G (p.Leu570Val) rs876657966
NM_002880.4(RAF1):c.1720_1760dup (p.Asp587_Cys588insIleArgThrAlaProLysGlnTer) rs2058275378
NM_002880.4(RAF1):c.1724A>C (p.Lys575Thr) rs767890715
NM_002880.4(RAF1):c.172A>C (p.Ile58Leu) rs147984543
NM_002880.4(RAF1):c.1770G>C (p.Lys590Asn) rs773583951
NM_002880.4(RAF1):c.1842G>A (p.Pro614=) rs200235582
NM_002880.4(RAF1):c.1927C>T (p.Pro643Ser) rs876657967
NM_002880.4(RAF1):c.207+10C>T rs2059446210
NM_002880.4(RAF1):c.226A>G (p.Met76Val) rs730880999
NM_002880.4(RAF1):c.237T>G (p.His79Gln) rs876661384
NM_002880.4(RAF1):c.321-4delinsTG rs2125421173
NM_002880.4(RAF1):c.325_327del (p.Lys109del) rs1418886913
NM_002880.4(RAF1):c.329C>T (p.Ala110Val) rs397516819
NM_002880.4(RAF1):c.379C>G (p.Gln127Glu) rs397516820
NM_002880.4(RAF1):c.388T>A (p.Phe130Ile) rs397516821
NM_002880.4(RAF1):c.419A>G (p.Asn140Ser) rs876657968
NM_002880.4(RAF1):c.424G>T (p.Ala142Ser) rs1553614748
NM_002880.4(RAF1):c.512A>G (p.Lys171Arg) rs876657969
NM_002880.4(RAF1):c.68_70del (p.Asp23del) rs749549707
NM_002880.4(RAF1):c.752T>A (p.Leu251His) rs1553613787
NM_002880.4(RAF1):c.775T>G (p.Ser259Ala) rs3730271
NM_002880.4(RAF1):c.776C>A (p.Ser259Tyr) rs397516827
NM_002880.4(RAF1):c.784A>C (p.Asn262His) rs1575573204
NM_002880.4(RAF1):c.837T>A (p.Asp279Glu) rs2125381916
NM_002880.4(RAF1):c.856G>A (p.Glu286Lys) rs147453956
NM_002880.4(RAF1):c.991-17A>G
Single allele

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