"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "RAF1"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 642037	NC_000003.11:g.(?_12626003)_(12660230_?)dup	LOC129389024, RAF1	Duplication	RASopathy	GUncertain significance
Select item 853114	NM_002880.4(RAF1):c.1947G>A (p.Ter649=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy +1 more	GLikely benign
Select item 1497081	NM_002880.4(RAF1):c.1943T>C (p.Phe648Ser)	RAF1 (F567S +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 44623	NM_002880.4(RAF1):c.1941C>T (p.Val647=)	MKRN2, RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GBenignFDA Recognized database
Select item 181516	NM_002880.4(RAF1):c.1939G>A (p.Val647Ile)	RAF1 (V647I +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2032474	NM_002880.4(RAF1):c.1938T>C (p.Pro646=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 411093	NM_002880.4(RAF1):c.1936C>T (p.Pro646Ser)	RAF1 (P646S +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 702984	NM_002880.4(RAF1):c.1929G>A (p.Pro643=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	Cardiovascular phenotype +1 more	GLikely benign
Select item 849719	NM_002880.4(RAF1):c.1928C>T (p.Pro643Leu)	RAF1 (P582L +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy +1 more	GUncertain significance
Select item 2069846	NM_002880.4(RAF1):c.1926C>G (p.Ser642=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 1144266	NM_002880.4(RAF1):c.1923G>A (p.Thr641=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy +1 more	GLikely benign
Select item 142298	NM_002880.4(RAF1):c.1922C>T (p.Thr641Met)	RAF1 (T641M +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 992259	NM_002880.4(RAF1):c.1921A>G (p.Thr641Ala)	RAF1 (T527A +5 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GUncertain significance
Select item 1782601	NM_002880.4(RAF1):c.1917G>A (p.Leu639=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy +1 more	GLikely benign
Select item 40628	NM_002880.4(RAF1):c.1914G>A (p.Thr638=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GBenignFDA Recognized database
Select item 181515	NM_002880.4(RAF1):c.1913C>T (p.Thr638Met)	RAF1 (T638M +5 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 928753	NM_002880.4(RAF1):c.1910G>A (p.Cys637Tyr)	RAF1 (C523Y +5 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GUncertain significance
Select item 1655234	NM_002880.4(RAF1):c.1905T>C (p.Asn635=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 577199	NM_002880.4(RAF1):c.1904A>G (p.Asn635Ser)	RAF1 (N635S +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 641642	NM_002880.4(RAF1):c.1901T>C (p.Ile634Thr)	RAF1 (I601T +5 more)	Single nucleotide variant (missense variant +1 more)	Noonan syndrome 5 +2 more	GUncertain significance
Select item 742213	NM_002880.4(RAF1):c.1899T>C (p.Asp633=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 2065031	NM_002880.4(RAF1):c.1898A>G (p.Asp633Gly)	RAF1 (D519G +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 2046784	NM_002880.4(RAF1):c.1896G>A (p.Glu632=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 1976440	NM_002880.4(RAF1):c.1894G>A (p.Glu632Lys)	RAF1 (E599K +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 2892459	NM_002880.4(RAF1):c.1891A>G (p.Thr631Ala)	RAF1 (T631A +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 1474502	NM_002880.4(RAF1):c.1886C>G (p.Ala629Gly)	RAF1 (A515G +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 864448	NM_002880.4(RAF1):c.1885G>T (p.Ala629Ser)	RAF1 (A515S +5 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 181514	NM_002880.4(RAF1):c.1880G>A (p.Arg627Gln)	RAF1 (R627Q +5 more)	Single nucleotide variant (missense variant +1 more)	Dilated cardiomyopathy 1NN +2 more	GUncertain significance
Select item 181513	NM_002880.4(RAF1):c.1879C>T (p.Arg627Trp)	RAF1 (R627W +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GUncertain significance
Select item 520554	NM_002880.4(RAF1):c.1877A>G (p.His626Arg)	RAF1 (H626R +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1987344	NM_002880.4(RAF1):c.1875G>A (p.Leu625=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy +1 more	GLikely benign
Select item 391813	NM_002880.4(RAF1):c.1871C>G (p.Ser624Cys)	RAF1 (S624C +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 3018277	NM_002880.4(RAF1):c.1869A>G (p.Pro623=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 393135	NM_002880.4(RAF1):c.1867C>T (p.Pro623Ser)	RAF1 (P623S +5 more)	Single nucleotide variant (missense variant +1 more)	LEOPARD syndrome 2 +4 more	GUncertain significance
Select item 2815921	NM_002880.4(RAF1):c.1863C>G (p.Ser621=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 767462	NM_002880.4(RAF1):c.1863C>T (p.Ser621=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	Cardiovascular phenotype +1 more	GLikely benign
Select item 949432	NM_002880.4(RAF1):c.1858G>A (p.Ala620Thr)	RAF1 (A587T +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 518752	NM_002880.4(RAF1):c.1857C>T (p.Ser619=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy +1 more	GLikely benign
Select item 2132528	NM_002880.4(RAF1):c.1854G>C (p.Arg618=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 1413764	NM_002880.4(RAF1):c.1852C>T (p.Arg618Trp)	RAF1 (R537W +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 1022960	NM_002880.4(RAF1):c.1850A>G (p.Asn617Ser)	RAF1 (N503S +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3000160	NM_002880.4(RAF1):c.1848C>T (p.Ile616=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 928752	NM_002880.4(RAF1):c.1842G>A (p.Pro614=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 561771	NM_002880.4(RAF1):c.1842G>C (p.Pro614=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GLikely benign
Select item 2825043	NM_002880.4(RAF1):c.1841C>T (p.Pro614Leu)	RAF1 (P533L +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 1404139	NM_002880.4(RAF1):c.1837_1838del (p.Leu613fs)	RAF1 (L532fs +5 more)	Microsatellite (frameshift variant +1 more)	RASopathy	GUncertain significance
Select item 13960	NM_002880.4(RAF1):c.1837C>G (p.Leu613Val)	RAF1 (L613V +5 more)	Single nucleotide variant (missense variant +1 more)	Noonan syndrome	GPathogenicFDA Recognized database
Select item 1781050	NM_002880.4(RAF1):c.1836T>C (p.Ser612=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy +1 more	GLikely benign
Select item 1038077	NM_002880.4(RAF1):c.1835C>G (p.Ser612Cys)	RAF1 (S551C +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 2734444	NM_002880.4(RAF1):c.1834T>A (p.Ser612Thr)	RAF1 (S498T +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 863502	NM_002880.4(RAF1):c.1832A>C (p.His611Pro)	RAF1 (H497P +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 40627	NM_002880.4(RAF1):c.1830A>G (p.Gln610=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GBenignFDA Recognized database
Select item 2159569	NM_002880.4(RAF1):c.1822C>G (p.Leu608Val)	RAF1 (L494V +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 699817	NM_002880.4(RAF1):c.1821G>A (p.Glu607=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy +3 more	GBenign/Likely benign
Select item 181512	NM_002880.4(RAF1):c.1814C>T (p.Ser605Phe)	RAF1 (S605F +5 more)	Single nucleotide variant (missense variant +1 more)	not provided +6 more	GUncertain significance
Select item 1971876	NM_002880.4(RAF1):c.1811C>T (p.Ser604Phe)	RAF1 (S523F +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 1567479	NM_002880.4(RAF1):c.1807C>T (p.Leu603=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 1394381	NM_002880.4(RAF1):c.1807C>A (p.Leu603Met)	RAF1 (L542M +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 2878772	NM_002880.4(RAF1):c.1806C>A (p.Ile602=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 2957933	NM_002880.4(RAF1):c.1804-7_1804-4del	RAF1	Deletion (intron variant)	RASopathy	GLikely benign
Select item 165004	NM_002880.3(RAF1):c.1804-11_1804-7dup	RAF1	Duplication (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1952631	NM_002880.4(RAF1):c.1804-7G>C	RAF1	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 1078894	NM_002880.4(RAF1):c.1804-9_1804-8del	RAF1	Deletion (intron variant)	RASopathy	GLikely benign
Select item 2916837	NM_002880.4(RAF1):c.1804-13G>C	RAF1	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2843262	NM_002880.4(RAF1):c.1804-16T>G	RAF1	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2896324	NM_002880.4(RAF1):c.1803+20_1803+30del	RAF1	Deletion (intron variant)	RASopathy	GLikely benign
Select item 2784624	NM_002880.4(RAF1):c.1803+20G>C	RAF1	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2185949	NM_002880.4(RAF1):c.1803+18T>C	RAF1	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2898367	NM_002880.4(RAF1):c.1803+16G>A	RAF1	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 1638244	NM_002880.4(RAF1):c.1803+15T>G	RAF1	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2723016	NM_002880.4(RAF1):c.1803+13del	RAF1	Deletion (intron variant)	RASopathy	GLikely benign
Select item 1133591	NM_002880.4(RAF1):c.1803+9C>T	RAF1	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 515165	NM_002880.4(RAF1):c.1803+6G>C	RAF1	Single nucleotide variant (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1572430	NM_002880.4(RAF1):c.1800C>T (p.Pro600=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 2100649	NM_002880.4(RAF1):c.1799C>G (p.Pro600Arg)	RAF1 (P519R +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 1544117	NM_002880.4(RAF1):c.1794T>A (p.Leu598=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 1469736	NM_002880.4(RAF1):c.1784A>C (p.Glu595Ala)	RAF1 (E481A +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 517341	NM_002880.4(RAF1):c.1770G>C (p.Lys590Asn)	RAF1 (K590N +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy +4 more	GUncertain significance
Select item 1014430	NM_002880.4(RAF1):c.1768A>G (p.Lys590Glu)	RAF1 (K476E +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 1501883	NM_002880.4(RAF1):c.1765_1767del (p.Val589del)	RAF1 (V508del +5 more)	Deletion (inframe_deletion +1 more)	RASopathy	GUncertain significance
Select item 2740298	NM_002880.4(RAF1):c.1764T>C (p.Cys588=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 40626	NM_002880.4(RAF1):c.1755A>G (p.Val585=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GBenignFDA Recognized database
Select item 836090	NM_002880.4(RAF1):c.1746G>C (p.Lys582Asn)	RAF1 (K549N +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 577639	NM_002880.4(RAF1):c.1741A>G (p.Met581Val)	RAF1 (M581V +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy +2 more	GUncertain significance
Select item 1719393	NM_002880.4(RAF1):c.1738G>T (p.Ala580Ser)	RAF1 (A466S +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 2078404	NM_002880.4(RAF1):c.1734C>T (p.Pro578=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 1919677	NM_002880.4(RAF1):c.1725G>C (p.Lys575Asn)	RAF1 (K461N +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 1910939	NM_002880.4(RAF1):c.1725G>A (p.Lys575=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 177842	NM_002880.4(RAF1):c.1721A>G (p.Tyr574Cys)	RAF1 (Y574C +5 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +7 more	GConflicting classifications of pathogenicity
Select item 2143749	NM_002880.4(RAF1):c.1719A>G (p.Leu573=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 2696773	NM_002880.4(RAF1):c.1713T>C (p.Ser571=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 843965	NM_002880.4(RAF1):c.1706_1712dup (p.Ser571delinsArgSerTer)	RAF1	Duplication (nonsense +1 more)	RASopathy	GUncertain significance
Select item 1640632	NM_002880.4(RAF1):c.1710T>G (p.Leu570=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy	GLikely benign
Select item 698911	NM_002880.4(RAF1):c.1704A>G (p.Pro568=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy +2 more	GLikely benign
Select item 44622	NM_002880.4(RAF1):c.1695T>C (p.Tyr565=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	RASopathy +1 more	GLikely benign
Select item 639241	NM_002880.4(RAF1):c.1694A>G (p.Tyr565Cys)	RAF1 (Y484C +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy	GUncertain significance
Select item 518871	NM_002880.4(RAF1):c.1690G>A (p.Gly564Arg)	RAF1 (G564R +5 more)	Single nucleotide variant (missense variant +1 more)	RASopathy +1 more	GUncertain significance
Select item 516880	NM_002880.4(RAF1):c.1689A>G (p.Arg563=)	RAF1	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GLikely benign
Select item 179378	NM_002880.4(RAF1):c.1688G>A (p.Arg563Gln)	RAF1 (R563Q +5 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GUncertain significance
Select item 849037	NM_002880.4(RAF1):c.1687C>T (p.Arg563Ter)	RAF1 (R449* +5 more)	Single nucleotide variant (nonsense +1 more)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity

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