ClinVar for Gene (Select 6237) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3062398	GRCh37/hg19 19q13.33-13.41(chr19:48905537-51614930)x3	ACP4, ADM5 +118 more	Copy number gain	not specified	GLikely pathogenic
Select item 3039622	NM_006270.5(RRAS):c.39G>T (p.Arg13=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related condition	GLikely benign
Select item 3039282	NM_006270.5(RRAS):c.60G>C (p.Gly20=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related condition	GLikely benign
Select item 3039264	NM_006270.5(RRAS):c.57T>C (p.Pro19=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related condition	GLikely benign
Select item 3039001	NM_006270.5(RRAS):c.54A>C (p.Gly18=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related condition	GLikely benign
Select item 3014053	NM_006270.5(RRAS):c.262del (p.Glu88fs)	RRAS (E88fs)	Deletion (frameshift variant)	Noonan syndrome	GUncertain significance
Select item 2980147	NM_006270.5(RRAS):c.153+18G>A	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2971617	NM_006270.5(RRAS):c.576A>G (p.Lys192=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome	GUncertain significance
Select item 2962737	NM_006270.5(RRAS):c.533A>C (p.Asn178Thr)	RRAS (N178T)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2911862	NM_006270.5(RRAS):c.241+20A>G	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2911366	NM_006270.5(RRAS):c.253G>A (p.Ala85Thr)	RRAS (A85T)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2885165	NM_006270.5(RRAS):c.345-5C>T	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2816216	NM_006270.5(RRAS):c.28G>A (p.Gly10Arg)	RRAS (G10R)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2813332	NM_006270.5(RRAS):c.367T>A (p.Phe123Ile)	RRAS (F123I)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2813323	NM_006270.5(RRAS):c.573-16del	RRAS	Deletion (intron variant)	Noonan syndrome	GLikely benign
Select item 2798081	NM_006270.5(RRAS):c.241+17T>C	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2753853	NM_006270.5(RRAS):c.454-11C>G	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2746151	NM_006270.5(RRAS):c.154-10A>T	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2733390	NM_006270.5(RRAS):c.289T>C (p.Tyr97His)	RRAS (Y97H)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2730479	NM_006270.5(RRAS):c.567T>C (p.Ala189=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome	GLikely benign
Select item 2729790	NM_006270.5(RRAS):c.516G>T (p.Ser172=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome	GLikely benign
Select item 2725877	NM_006270.5(RRAS):c.154-6C>T	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2725369	NM_006270.5(RRAS):c.609C>T (p.Pro203=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GLikely benign
Select item 2716092	NM_006270.5(RRAS):c.454-20C>T	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2715700	NM_006270.5(RRAS):c.274G>A (p.Ala92Thr)	RRAS (A92T)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2698124	NM_006270.5(RRAS):c.182C>A (p.Thr61Asn)	RRAS (T61N)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2684892	GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	ACP4, ADM5 +261 more	Copy number gain	not provided	GLikely pathogenic
Select item 2672155	NM_006270.5(RRAS):c.259C>G (p.Gln87Glu)	RRAS (Q87E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2637823	NM_006270.5(RRAS):c.355G>A (p.Val119Met)	RRAS (V119M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2631818	NM_006270.5(RRAS):c.9C>G (p.Ser3Arg)	RRAS (S3R)	Single nucleotide variant (missense variant)	RRAS-related condition	GUncertain significance
Select item 2627312	NM_006270.5(RRAS):c.454-13C>T	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome +1 more	GLikely benign
Select item 2624545	NM_006270.5(RRAS):c.571C>G (p.Arg191Gly)	RRAS (R191G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2564299	NM_006270.5(RRAS):c.12G>A (p.Gly4=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 2564298	NM_006270.5(RRAS):c.13G>A (p.Ala5Thr)	RRAS (A5T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2564297	NM_006270.5(RRAS):c.95T>A (p.Leu32Gln)	RRAS (L32Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2564296	NM_006270.5(RRAS):c.375G>A (p.Gln125=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 2564295	NM_006270.5(RRAS):c.319G>A (p.Val107Met)	RRAS (V107M)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2506325	NM_006270.5(RRAS):c.*5G>A	RRAS	Single nucleotide variant (3 prime UTR variant)	RRAS-related condition +1 more	GConflicting classifications of pathogenicity
Select item 2497326	NM_006270.5(RRAS):c.334G>T (p.Asp112Tyr)	RRAS (D112Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2449550	NM_006270.5(RRAS):c.507T>C (p.Phe169=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 2449548	NM_006270.5(RRAS):c.275C>T (p.Ala92Val)	RRAS (A92V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2417016	NM_006270.5(RRAS):c.572+3G>A	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GUncertain significance
Select item 2382698	NM_006270.5(RRAS):c.613G>A (p.Ala205Thr)	RRAS (A205T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2361108	NM_006270.5(RRAS):c.449G>A (p.Arg150His)	RRAS (R150H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2329702	NM_006270.5(RRAS):c.349A>T (p.Asn117Tyr)	RRAS (N117Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2203117	NM_006270.5(RRAS):c.50G>T (p.Gly17Val)	RRAS (G17V)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2199243	NM_006270.5(RRAS):c.337C>T (p.Arg113Trp)	RRAS (R113W)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2196936	NM_006270.5(RRAS):c.242-8C>G	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2194767	NM_006270.5(RRAS):c.12_13delinsAA (p.Ala5Thr)	RRAS (A5T)	Indel (missense variant)	Noonan syndrome	GUncertain significance
Select item 2193595	NM_006270.5(RRAS):c.288G>A (p.Gln96=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome	GLikely benign
Select item 2145313	NM_006270.5(RRAS):c.242-12_242-11del	RRAS	Deletion (intron variant)	Noonan syndrome	GLikely benign
Select item 2144588	NM_006270.5(RRAS):c.209G>A (p.Cys70Tyr)	RRAS (C70Y)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 2144172	NM_006270.5(RRAS):c.493C>G (p.His165Asp)	RRAS (H165D)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2137439	NM_006270.5(RRAS):c.1A>T (p.Met1Leu)	RRAS (M1L)	Single nucleotide variant (missense variant +1 more)	Noonan syndrome	GUncertain significance
Select item 2132901	NM_006270.5(RRAS):c.572+13C>A	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2131899	NM_006270.5(RRAS):c.643T>C (p.Cys215Arg)	RRAS (C215R)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2118815	NM_006270.5(RRAS):c.572+5G>A	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GUncertain significance
Select item 2087843	NM_006270.5(RRAS):c.453+17T>C	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2083076	NM_006270.5(RRAS):c.571C>T (p.Arg191Trp)	RRAS (R191W)	Single nucleotide variant (missense variant)	Noonan syndrome +2 more	GUncertain significance
Select item 2072335	NM_006270.5(RRAS):c.84G>C (p.Glu28Asp)	RRAS (E28D)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2059832	NM_006270.5(RRAS):c.599C>T (p.Pro200Leu)	RRAS (P200L)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2057672	NM_006270.5(RRAS):c.345-14G>A	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GUncertain significance
Select item 2051891	NM_006270.5(RRAS):c.454-4C>T	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2051586	NM_006270.5(RRAS):c.541G>A (p.Glu181Lys)	RRAS (E181K)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2039989	NM_006270.5(RRAS):c.573-15G>A	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 2039752	NM_006270.5(RRAS):c.610A>G (p.Ser204Gly)	RRAS (S204G)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2038116	NM_006270.5(RRAS):c.44G>C (p.Arg15Pro)	RRAS (R15P)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 2015833	NM_006270.5(RRAS):c.292A>G (p.Met98Val)	RRAS (M98V)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 1995598	NM_006270.5(RRAS):c.44G>A (p.Arg15Gln)	RRAS (R15Q)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 1977857	NM_006270.5(RRAS):c.153+10C>A	RRAS	Single nucleotide variant (intron variant)	Noonan syndrome	GLikely benign
Select item 1966469	NM_006270.5(RRAS):c.436C>A (p.Leu146Met)	RRAS (L146M)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 1964939	NM_006270.5(RRAS):c.480C>T (p.Phe160=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 1964490	NM_006270.5(RRAS):c.1A>G (p.Met1Val)	RRAS (M1V)	Single nucleotide variant (missense variant +1 more)	Noonan syndrome	GUncertain significance
Select item 1946820	NM_006270.5(RRAS):c.454-10dup	RRAS	Duplication (intron variant)	Noonan syndrome	GBenign
Select item 1943632	NM_006270.5(RRAS):c.295C>T (p.Arg99Cys)	RRAS (R99C)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1906713	NM_006270.5(RRAS):c.454G>A (p.Val152Ile)	RRAS (V152I)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 1805320	NM_006270.5(RRAS):c.43C>T (p.Arg15Trp)	RRAS (R15W)	Single nucleotide variant (missense variant)	Noonan syndrome	GUncertain significance
Select item 1799468	NM_006270.5(RRAS):c.306C>T (p.His102=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GLikely benign
Select item 1795425	NM_006270.5(RRAS):c.273G>T (p.Gly91=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1795046	NM_006270.5(RRAS):c.270C>T (p.Phe90=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 1792928	NM_006270.5(RRAS):c.254C>T (p.Ala85Val)	RRAS (A85V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1792659	NM_006270.5(RRAS):c.252C>T (p.Thr84=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GLikely benign
Select item 1787743	NM_006270.5(RRAS):c.220G>A (p.Gly74Ser)	RRAS (G74S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1787064	NM_006270.5(RRAS):c.216G>A (p.Val72=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1776790	NM_006270.5(RRAS):c.162C>T (p.Phe54=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 1765039	NM_006270.5(RRAS):c.88C>G (p.His30Asp)	RRAS (H30D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1759736	NM_006270.5(RRAS):c.75G>A (p.Pro25=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1756600	NM_006270.5(RRAS):c.6C>T (p.Ser2=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1756044	NM_006270.5(RRAS):c.68A>C (p.Asp23Ala)	RRAS (D23A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1753472	NM_006270.5(RRAS):c.642C>T (p.Pro214=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GLikely benign
Select item 1752782	NM_006270.5(RRAS):c.630C>T (p.Gly210=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GLikely benign
Select item 1752755	NM_006270.5(RRAS):c.121G>A (p.Gly41Ser)	RRAS (G41S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1752712	NM_006270.5(RRAS):c.62C>T (p.Pro21Leu)	RRAS (P21L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1752208	NM_006270.5(RRAS):c.620G>A (p.Arg207Lys)	RRAS (R207K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1751604	NM_006270.5(RRAS):c.60G>A (p.Gly20=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1750107	NM_006270.5(RRAS):c.585A>G (p.Glu195=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1749772	NM_006270.5(RRAS):c.57T>G (p.Pro19=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1747933	NM_006270.5(RRAS):c.54A>G (p.Gly18=)	RRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1747302	NM_006270.5(RRAS):c.53G>T (p.Gly18Val)	RRAS (G18V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1744580	NM_006270.5(RRAS):c.498G>A (p.Val166=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GConflicting classifications of pathogenicity

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