"Ambry Genetics"[submitter] AND "MRAS"[gene] - ClinVar

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Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1427167	NM_001085049.3(MRAS):c.12C>T (p.Ser4=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +1 more	GLikely benign
Select item 1539564	NM_001085049.3(MRAS):c.15C>T (p.Ala5=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1413231	NM_001085049.3(MRAS):c.16G>A (p.Val6Ile)	MRAS (V6I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GUncertain significance
Select item 496408	NM_001085049.3(MRAS):c.22A>G (p.Ser8Gly)	MRAS (S8G)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1483022	NM_001085049.3(MRAS):c.29A>G (p.Asn10Ser)	MRAS (N10S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2793297	NM_001085049.3(MRAS):c.42C>T (p.Tyr14=)	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 1657756	NM_001085049.3(MRAS):c.66G>T (p.Gly22=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 986261	NM_001085049.3(MRAS):c.80G>C (p.Ser27Thr)	MRAS (S27T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1750105	NM_001085049.3(MRAS):c.120T>G (p.Pro40=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases	GLikely benign
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 1565091	NM_001085049.3(MRAS):c.159T>C (p.His53=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +1 more	GLikely benign
Select item 1466598	NM_001085049.3(MRAS):c.162G>A (p.Thr54=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	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 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 1542609	NM_001085049.3(MRAS):c.189G>A (p.Leu63=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1782840	NM_001085049.3(MRAS):c.192C>T (p.Asp64=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	MRAS-related condition +2 more	GConflicting classifications of pathogenicity
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 985724	NM_001085049.3(MRAS):c.197T>A (p.Leu66Gln)	MRAS (L66Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1547407	NM_001085049.3(MRAS):c.225C>T (p.Ser75=)	MRAS	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +1 more	GLikely benign
Select item 928788	NM_001085049.3(MRAS):c.252G>A (p.Thr84=)	MRAS	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 1793082	NM_001085049.3(MRAS):c.255G>A (p.Gly85=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1794660	NM_001085049.3(MRAS):c.267C>T (p.Leu89=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +1 more	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 1795174	NM_001085049.3(MRAS):c.271G>A (p.Val91Ile)	MRAS (V91I +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	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 929025	NM_001085049.3(MRAS):c.291G>A (p.Lys97=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1445338	NM_001085049.3(MRAS):c.300T>A (p.Phe100Leu)	MRAS (F24L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
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 496409	NM_001085049.3(MRAS):c.306C>T (p.His102=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1601704	NM_001085049.3(MRAS):c.330C>T (p.Ile110=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 1486644	NM_001085049.3(MRAS):c.332T>G (p.Leu111Arg)	MRAS (L111R +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1730710	NM_001085049.3(MRAS):c.336C>T (p.Arg112=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 1730697	NM_001085049.3(MRAS):c.336C>A (p.Arg112=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1730809	NM_001085049.3(MRAS):c.337G>A (p.Val113Ile)	MRAS (V37I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	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 1568129	NM_001085049.3(MRAS):c.360G>A (p.Pro120=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 1321384	NM_001085049.3(MRAS):c.369C>T (p.Leu123=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 2562166	NM_001085049.3(MRAS):c.377A>G (p.Asn126Ser)	MRAS (N126S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1430569	NM_001085049.3(MRAS):c.378C>A (p.Asn126Lys)	MRAS (N126K +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1737189	NM_001085049.3(MRAS):c.402G>A (p.Arg134=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1552421	NM_001085049.3(MRAS):c.411C>G (p.Thr137=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 1738488	NM_001085049.3(MRAS):c.417G>A (p.Glu139=)	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 1621797	NM_001085049.3(MRAS):c.441A>G (p.Lys147=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 496410	NM_001085049.3(MRAS):c.453G>A (p.Pro151=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
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 3226221	NM_001085049.3(MRAS):c.465C>T (p.Thr155=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 1746862	NM_001085049.3(MRAS):c.532C>A (p.Gln178Lys)	MRAS (Q178K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	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 1603823	NM_001085049.3(MRAS):c.540G>A (p.Pro180=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 981089	NM_001085049.3(MRAS):c.548G>A (p.Ser183Asn)	MRAS (S107N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
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 1749598	NM_001085049.3(MRAS):c.577C>T (p.Arg193Trp)	MRAS (R193W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1749649	NM_001085049.3(MRAS):c.578G>A (p.Arg193Gln)	MRAS (R117Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1750310	NM_001085049.3(MRAS):c.588G>A (p.Arg196=)	MRAS	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
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 1626034	NM_001085049.3(MRAS):c.609G>A (p.Leu203=)	MRAS	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign

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Items: 58