ClinVar for Gene (Select 22808) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3361322	NM_001085049.3(MRAS):c.413G>A (p.Arg138Lys)	MRAS (R138K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3295785	NM_001085049.3(MRAS):c.254G>A (p.Gly85Glu)	MRAS (G9E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3295784	NM_001085049.3(MRAS):c.593C>G (p.Thr198Arg)	MRAS (T122R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3247008	NC_000003.11:g.(?_138116146)_(138121111_?)dup	MRAS	Duplication	not provided	GUncertain significance
Select item 3226221	NM_001085049.3(MRAS):c.465C>T (p.Thr155=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3226220	NM_001085049.3(MRAS):c.429A>G (p.Glu143=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3226219	NM_001085049.3(MRAS):c.182C>T (p.Ala61Val)	MRAS (A61V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3226218	NM_001085049.3(MRAS):c.130C>T (p.Pro44Ser)	MRAS (P44S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3016270	NM_001085049.3(MRAS):c.248G>A (p.Arg83His)	MRAS (R7H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3010161	NM_001085049.3(MRAS):c.431T>C (p.Met144Thr)	MRAS (M144T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3008671	NM_001085049.3(MRAS):c.331C>T (p.Leu111=)	MRAS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3005145	NM_001085049.3(MRAS):c.232C>T (p.Arg78Trp)	MRAS (R2W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2997186	NM_001085049.3(MRAS):c.348-4C>T	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2993630	NM_001085049.3(MRAS):c.307G>A (p.Val103Met)	MRAS (V103M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2992622	NM_001085049.3(MRAS):c.251C>T (p.Thr84Met)	MRAS (T84M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2991993	NM_001085049.3(MRAS):c.293C>A (p.Ala98Asp)	MRAS (A22D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2985969	NM_001085049.3(MRAS):c.493G>A (p.Asp165Asn)	MRAS (D89N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2967110	NM_001085049.3(MRAS):c.447+12C>T	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2900922	NM_001085049.3(MRAS):c.347+3G>A	MRAS	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2871575	NM_001085049.3(MRAS):c.114T>C (p.Phe38=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2864550	NM_001085049.3(MRAS):c.38C>T (p.Thr13Ile)	MRAS (T13I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2856949	NM_001085049.3(MRAS):c.500_508dup (p.His169_Asp170insAlaPheHis)	MRAS	Duplication (inframe_insertion)	not provided	GUncertain significance
Select item 2854215	NM_001085049.3(MRAS):c.292G>A (p.Ala98Thr)	MRAS (A22T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2850862	NM_001085049.3(MRAS):c.348-13C>G	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2847741	NM_001085049.3(MRAS):c.314G>A (p.Arg105His)	MRAS (R29H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2835266	NM_001085049.3(MRAS):c.527+18C>T	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2832035	NM_001085049.3(MRAS):c.171C>T (p.Asp57=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2824421	NM_001085049.3(MRAS):c.527+10G>A	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2821711	NM_001085049.3(MRAS):c.84C>A (p.Ala28=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2820239	NM_001085049.3(MRAS):c.510C>A (p.Asp170Glu)	MRAS (D170E +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2819695	NM_001085049.3(MRAS):c.121_124del (p.Asp41fs)	MRAS (D41fs)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2808171	NM_001085049.3(MRAS):c.276C>T (p.Tyr92=)	MRAS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2798283	NM_001085049.3(MRAS):c.173A>G (p.Asn58Ser)	MRAS (N58S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2793297	NM_001085049.3(MRAS):c.42C>T (p.Tyr14=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +1 more	GLikely benign
Select item 2786088	NM_001085049.3(MRAS):c.30C>T (p.Asn10=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2779328	NM_001085049.3(MRAS):c.506A>G (p.His169Arg)	MRAS (H93R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2736858	NM_001085049.3(MRAS):c.36C>T (p.Pro12=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2700576	NM_001085049.3(MRAS):c.348-17G>C	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2697294	NM_001085049.3(MRAS):c.527+9T>C	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2694483	NM_001085049.3(MRAS):c.160dup (p.Thr54fs)	MRAS (T54fs)	Duplication (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2686009	NM_001085049.3(MRAS):c.359C>T (p.Pro120Leu)	MRAS (P120L +1 more)	Single nucleotide variant (missense variant)	Male infertility with azoospermia or oligozoospermia due to single gene mutation	GLikely pathogenic
Select item 2671581	Single allele	TFDP2, TRIM42 +26 more	Deletion	not provided	GPathogenic
Select item 2662976	NM_001085049.3(MRAS):c.196C>G (p.Leu66Val)	MRAS (L66V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2654189	NM_001085049.3(MRAS):c.335G>A (p.Arg112His)	MRAS (R112H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2596480	NM_001085049.3(MRAS):c.539C>T (p.Pro180Leu)	MRAS (P104L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2565773	NM_001085049.3(MRAS):c.456C>T (p.Tyr152=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 2562166	NM_001085049.3(MRAS):c.377A>G (p.Asn126Ser)	MRAS (N126S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2562165	NM_001085049.3(MRAS):c.196C>T (p.Leu66=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2451217	NM_001085049.3(MRAS):c.45G>A (p.Lys15=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2451215	NM_001085049.3(MRAS):c.165G>C (p.Glu55Asp)	MRAS (E55D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2451214	NM_001085049.3(MRAS):c.601C>T (p.His201Tyr)	MRAS (H201Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2426786	NC_000003.11:g.(?_137781658)_(138665815_?)del	A4GNT, ARMC8 +9 more	Deletion	not provided	GPathogenic
Select item 2179682	NM_001085049.3(MRAS):c.567A>C (p.Lys189Asn)	MRAS (K113N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2135815	NM_001085049.3(MRAS):c.271G>C (p.Val91Leu)	MRAS (V15L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2127892	NM_001085049.3(MRAS):c.161C>T (p.Thr54Met)	MRAS (T54M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2123987	NM_001085049.3(MRAS):c.527+17C>T	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2120154	NM_001085049.3(MRAS):c.557A>C (p.Lys186Thr)	MRAS (K186T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2118744	NM_001085049.3(MRAS):c.538C>G (p.Pro180Ala)	MRAS (P104A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2118379	NM_001085049.3(MRAS):c.527+14T>G	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2114586	NM_001085049.3(MRAS):c.528-13A>G	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2107536	NM_001085049.3(MRAS):c.348-19C>T	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2105633	NM_001085049.3(MRAS):c.334C>T (p.Arg112Cys)	MRAS (R112C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2100316	NM_001085049.3(MRAS):c.347+13G>A	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2092912	NM_001085049.3(MRAS):c.85C>T (p.Leu29Phe)	MRAS (L29F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2089272	NM_001085049.3(MRAS):c.446A>G (p.Asn149Ser)	MRAS (N73S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2088034	NM_001085049.3(MRAS):c.282C>T (p.Val94=)	MRAS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2087621	NM_001085049.3(MRAS):c.447+19G>A	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2081116	NM_001085049.3(MRAS):c.621C>A (p.Ile207=)	MRAS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2080808	NM_001085049.3(MRAS):c.608T>G (p.Leu203Arg)	MRAS (L203R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2031838	NM_001085049.3(MRAS):c.372G>T (p.Val124=)	MRAS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2017761	NM_001085049.3(MRAS):c.537T>G (p.Ile179Met)	MRAS (I179M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2017736	NM_001085049.3(MRAS):c.275A>C (p.Tyr92Ser)	MRAS (Y92S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2017169	NM_001085049.3(MRAS):c.184A>G (p.Ile62Val)	MRAS (I62V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2011763	NM_001085049.3(MRAS):c.39A>G (p.Thr13=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1999353	NM_001085049.3(MRAS):c.347+4A>G	MRAS	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1996126	NM_001085049.3(MRAS):c.410C>T (p.Thr137Ile)	MRAS (T61I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1995675	NM_001085049.3(MRAS):c.348-10T>C	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1978228	NM_001085049.3(MRAS):c.586C>T (p.Arg196Trp)	MRAS (R120W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1970208	NM_001085049.3(MRAS):c.350A>G (p.Glu117Gly)	MRAS (E117G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1963013	NM_001085049.3(MRAS):c.194-10C>T	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1961451	NM_001085049.3(MRAS):c.23G>C (p.Ser8Thr)	MRAS (S8T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1960590	NM_001085049.3(MRAS):c.384C>T (p.Val128=)	MRAS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1956785	NM_001085049.3(MRAS):c.525T>A (p.Ile175=)	MRAS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1953841	NM_001085049.3(MRAS):c.347+10A>C	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1944788	NM_001085049.3(MRAS):c.270C>T (p.Ile90=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1935161	NM_001085049.3(MRAS):c.279C>T (p.Ser93=)	MRAS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1934954	NM_001085049.3(MRAS):c.514G>A (p.Val172Ile)	MRAS (V96I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1933910	NM_001085049.3(MRAS):c.612A>G (p.Gln204=)	MRAS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1929626	NM_001085049.3(MRAS):c.194-5C>T	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1924675	NM_001085049.3(MRAS):c.527+13C>A	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1924415	NM_001085049.3(MRAS):c.32T>C (p.Leu11Pro)	MRAS (L11P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1915958	NM_001085049.3(MRAS):c.447+15G>T	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1910470	NM_001085049.3(MRAS):c.348-15T>G	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1905798	NM_001085049.3(MRAS):c.447+13G>A	MRAS	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1904033	NM_001085049.3(MRAS):c.261C>T (p.Gly87=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1810726	NM_001085049.3(MRAS):c.27C>A (p.Asp9Glu)	MRAS (D9E)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1807815	GRCh37/hg19 3q13.31-26.31(chr3:116620308-172042292)x3	A4GNT, AADAC +303 more	Copy number gain	not provided	GPathogenic
Select item 1799335	NM_001085049.3(MRAS):c.305A>G (p.His102Arg)	MRAS (H26R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1796946	NM_001085049.3(MRAS):c.285T>C (p.Thr95=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1795174	NM_001085049.3(MRAS):c.271G>A (p.Val91Ile)	MRAS (V91I +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance

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