"Ambry Genetics"[submitter] AND "RRAS"[gene] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 1 to 100 of 112

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1557570	NM_006270.5(RRAS):c.652C>T (p.Leu218=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 1366588	NM_006270.5(RRAS):c.646G>A (p.Val216Ile)	RRAS (V216I)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1665914	NM_006270.5(RRAS):c.645C>T (p.Cys215=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 1753472	NM_006270.5(RRAS):c.642C>T (p.Pro214=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 582576	NM_006270.5(RRAS):c.631G>A (p.Gly211Arg)	RRAS (G211R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1752782	NM_006270.5(RRAS):c.630C>T (p.Gly210=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 849110	NM_006270.5(RRAS):c.627G>T (p.Lys209Asn)	RRAS (K209N)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 577262	NM_006270.5(RRAS):c.623A>G (p.Lys208Arg)	RRAS (K208R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1752208	NM_006270.5(RRAS):c.620G>A (p.Arg207Lys)	RRAS (R207K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225527	NM_006270.5(RRAS):c.616C>T (p.Pro206Ser)	RRAS (P206S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 934671	NM_006270.5(RRAS):c.614C>T (p.Ala205Val)	RRAS (A205V)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2382698	NM_006270.5(RRAS):c.613G>A (p.Ala205Thr)	RRAS (A205T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 457990	NM_006270.5(RRAS):c.600G>A (p.Pro200=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GBenign/Likely benign
Select item 3315390	NM_006270.5(RRAS):c.595C>A (p.Pro199Thr)	RRAS (P199T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1750107	NM_006270.5(RRAS):c.585A>G (p.Glu195=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3315391	NM_006270.5(RRAS):c.579C>T (p.Tyr193=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2624545	NM_006270.5(RRAS):c.571C>G (p.Arg191Gly)	RRAS (R191G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2083076	NM_006270.5(RRAS):c.571C>T (p.Arg191Trp)	RRAS (R191W)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 527794	NM_006270.5(RRAS):c.568G>C (p.Val190Leu)	RRAS (V190L)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2730479	NM_006270.5(RRAS):c.567T>C (p.Ala189=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GLikely benign
Select item 3225526	NM_006270.5(RRAS):c.563G>C (p.Arg188Pro)	RRAS (R188P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 928936	NM_006270.5(RRAS):c.563G>A (p.Arg188Gln)	RRAS (R188Q)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1103045	NM_006270.5(RRAS):c.543G>A (p.Glu181=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 1153600	NM_006270.5(RRAS):c.540C>T (p.Asp180=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 1015206	NM_006270.5(RRAS):c.533A>G (p.Asn178Ser)	RRAS (N178S)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 1471474	NM_006270.5(RRAS):c.527G>A (p.Arg176His)	RRAS (R176H)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 1554536	NM_006270.5(RRAS):c.516G>A (p.Ser172=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 705927	NM_006270.5(RRAS):c.516G>C (p.Ser172=)	RRAS	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 2449550	NM_006270.5(RRAS):c.507T>C (p.Phe169=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1744580	NM_006270.5(RRAS):c.498G>A (p.Val166=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1138642	NM_006270.5(RRAS):c.495C>T (p.His165=)	RRAS	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 3225524	NM_006270.5(RRAS):c.491A>T (p.His164Leu)	RRAS (H164L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1394417	NM_006270.5(RRAS):c.487T>C (p.Ser163Pro)	RRAS (S163P)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1743561	NM_006270.5(RRAS):c.484G>A (p.Ala162Thr)	RRAS (A162T)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 1743479	NM_006270.5(RRAS):c.483C>T (p.Gly161=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1964939	NM_006270.5(RRAS):c.480C>T (p.Phe160=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GLikely benign
Select item 1742099	NM_006270.5(RRAS):c.463T>C (p.Ser155Pro)	RRAS (S155P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1372718	NM_006270.5(RRAS):c.461G>A (p.Arg154Gln)	RRAS (R154Q)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2361108	NM_006270.5(RRAS):c.449G>A (p.Arg150His)	RRAS (R150H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1740467	NM_006270.5(RRAS):c.441G>A (p.Glu147=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1432373	NM_006270.5(RRAS):c.422G>C (p.Gly141Ala)	RRAS (G141A)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 1738729	NM_006270.5(RRAS):c.420C>T (p.Val140=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3156380	NM_006270.5(RRAS):c.412G>C (p.Val138Leu)	RRAS (V138L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 457988	NM_006270.5(RRAS):c.408C>T (p.Pro136=)	RRAS	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1736820	NM_006270.5(RRAS):c.399C>T (p.Asp133=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 707745	NM_006270.5(RRAS):c.396C>T (p.Arg132=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 1736508	NM_006270.5(RRAS):c.395G>A (p.Arg132His)	RRAS (R132H)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 848157	NM_006270.5(RRAS):c.394C>T (p.Arg132Cys)	RRAS (R132C)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 1735419	NM_006270.5(RRAS):c.383G>A (p.Arg128Gln)	RRAS (R128Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 457986	NM_006270.5(RRAS):c.379C>T (p.Leu127=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +2 more	GBenign/Likely benign
Select item 2564296	NM_006270.5(RRAS):c.375G>A (p.Gln125=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 773964	NM_006270.5(RRAS):c.372G>A (p.Thr124=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GBenign/Likely benign
Select item 527793	NM_006270.5(RRAS):c.371C>T (p.Thr124Met)	RRAS (T124M)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 1498730	NM_006270.5(RRAS):c.363G>A (p.Lys121=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 527795	NM_006270.5(RRAS):c.362A>G (p.Lys121Arg)	RRAS (K121R)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GBenign/Likely benign
Select item 854508	NM_006270.5(RRAS):c.352G>A (p.Glu118Lys)	RRAS (E118K)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 2329702	NM_006270.5(RRAS):c.349A>T (p.Asn117Tyr)	RRAS (N117Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 572125	NM_006270.5(RRAS):c.338G>A (p.Arg113Gln)	RRAS (R113Q)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 2497326	NM_006270.5(RRAS):c.334G>T (p.Asp112Tyr)	RRAS (D112Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1321403	NM_006270.5(RRAS):c.325G>A (p.Ala109Thr)	RRAS (A109T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1087744	NM_006270.5(RRAS):c.324C>T (p.Phe108=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 2564295	NM_006270.5(RRAS):c.319G>A (p.Val107Met)	RRAS (V107M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1799468	NM_006270.5(RRAS):c.306C>T (p.His102=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 1943632	NM_006270.5(RRAS):c.295C>T (p.Arg99Cys)	RRAS (R99C)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 2449548	NM_006270.5(RRAS):c.275C>T (p.Ala92Val)	RRAS (A92V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1795425	NM_006270.5(RRAS):c.273G>T (p.Gly91=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1795046	NM_006270.5(RRAS):c.270C>T (p.Phe90=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 706868	NM_006270.5(RRAS):c.255G>A (p.Ala85=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GBenign/Likely benign
Select item 1792928	NM_006270.5(RRAS):c.254C>T (p.Ala85Val)	RRAS (A85V)	Single nucleotide variant (missense variant)	not specified	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 457985	NM_006270.5(RRAS):c.243C>T (p.Ile81=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 1406870	NM_006270.5(RRAS):c.232C>T (p.Arg78Trp)	RRAS (R78W)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 527796	NM_006270.5(RRAS):c.231C>A (p.Ala77=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 933170	NM_006270.5(RRAS):c.229G>A (p.Ala77Thr)	RRAS (A77T)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1787743	NM_006270.5(RRAS):c.220G>A (p.Gly74Ser)	RRAS (G74S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1787064	NM_006270.5(RRAS):c.216G>A (p.Val72=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3315389	NM_006270.5(RRAS):c.211A>C (p.Ser71Arg)	RRAS (S71R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2144588	NM_006270.5(RRAS):c.209G>A (p.Cys70Tyr)	RRAS (C70Y)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 457984	NM_006270.5(RRAS):c.201G>A (p.Thr67=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 575349	NM_006270.5(RRAS):c.175G>C (p.Asp59His)	RRAS (D59H)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 527797	NM_006270.5(RRAS):c.174C>T (p.Tyr58=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +2 more	GBenign/Likely benign
Select item 573868	NM_006270.5(RRAS):c.167C>G (p.Ser56Cys)	RRAS (S56C)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1776790	NM_006270.5(RRAS):c.162C>T (p.Phe54=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 579337	NM_006270.5(RRAS):c.158A>T (p.Tyr53Phe)	RRAS (Y53F)	Single nucleotide variant (missense variant)	Noonan syndrome +1 more	GUncertain significance
Select item 1752755	NM_006270.5(RRAS):c.121G>A (p.Gly41Ser)	RRAS (G41S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 521665	NM_006270.5(RRAS):c.107GCG[5] (p.Gly39dup)	RRAS	Microsatellite (inframe_insertion)	Inborn genetic diseases	GLikely pathogenic
Select item 2564297	NM_006270.5(RRAS):c.95T>A (p.Leu32Gln)	RRAS (L32Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 842327	NM_006270.5(RRAS):c.94C>T (p.Leu32=)	RRAS	Single nucleotide variant (synonymous variant)	Noonan syndrome +1 more	GLikely benign
Select item 1765039	NM_006270.5(RRAS):c.88C>G (p.His30Asp)	RRAS (H30D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225529	NM_006270.5(RRAS):c.82G>A (p.Glu28Lys)	RRAS (E28K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1503389	NM_006270.5(RRAS):c.81C>T (p.Ser27=)	RRAS	Single nucleotide variant (synonymous variant)	RRAS-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 3225528	NM_006270.5(RRAS):c.79A>T (p.Ser27Cys)	RRAS (S27C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1759736	NM_006270.5(RRAS):c.75G>A (p.Pro25=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 642527	NM_006270.5(RRAS):c.74C>T (p.Pro25Leu)	RRAS (P25L)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1123565	NM_006270.5(RRAS):c.69C>T (p.Asp23=)	RRAS	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 1756044	NM_006270.5(RRAS):c.68A>C (p.Asp23Ala)	RRAS (D23A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1752712	NM_006270.5(RRAS):c.62C>T (p.Pro21Leu)	RRAS (P21L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1751604	NM_006270.5(RRAS):c.60G>A (p.Gly20=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1749772	NM_006270.5(RRAS):c.57T>G (p.Pro19=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1747933	NM_006270.5(RRAS):c.54A>G (p.Gly18=)	RRAS	Single nucleotide variant (synonymous variant)	not specified	GLikely benign

<< First< Prev

Page of 2