"PreventionGenetics, part of Exact Sciences"[submitter] AND "GPRASP2"[ - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2213119	NM_001004051.4(GPRASP2):c.63G>C (p.Glu21Asp)	ARMCX5-GPRASP2, GPRASP2 (E21D)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2378413	NM_001004051.4(GPRASP2):c.140G>C (p.Gly47Ala)	ARMCX5-GPRASP2, GPRASP2 (G47A)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3047223	NM_001004051.4(GPRASP2):c.264G>A (p.Thr88=)	ARMCX5-GPRASP2, GPRASP2	Single nucleotide variant (synonymous variant +1 more)	GPRASP2-related disorder	GLikely benign
Select item 3053315	NM_001004051.4(GPRASP2):c.326G>A (p.Arg109His)	ARMCX5-GPRASP2, GPRASP2 (R109H)	Single nucleotide variant (missense variant +1 more)	GPRASP2-related disorder	GLikely benign
Select item 3040660	NM_001004051.4(GPRASP2):c.504C>T (p.Gly168=)	ARMCX5-GPRASP2, GPRASP2	Single nucleotide variant (synonymous variant +1 more)	GPRASP2-related disorder	GLikely benign
Select item 3049800	NM_001004051.4(GPRASP2):c.585G>C (p.Trp195Cys)	ARMCX5-GPRASP2, GPRASP2 (W195C)	Single nucleotide variant (missense variant +1 more)	GPRASP2-related disorder	GLikely benign
Select item 3050159	NM_001004051.4(GPRASP2):c.698C>T (p.Ala233Val)	ARMCX5-GPRASP2, GPRASP2 (A233V)	Single nucleotide variant (missense variant +1 more)	GPRASP2-related disorder	GBenign
Select item 3039634	NM_001004051.4(GPRASP2):c.861G>A (p.Glu287=)	ARMCX5-GPRASP2, GPRASP2	Single nucleotide variant (synonymous variant +1 more)	GPRASP2-related disorder	GLikely benign
Select item 781553	NM_001004051.4(GPRASP2):c.865A>G (p.Ser289Gly)	ARMCX5-GPRASP2, GPRASP2 (S289G)	Single nucleotide variant (missense variant +1 more)	GPRASP2-related disorder +1 more	GBenign
Select item 781554	NM_001004051.4(GPRASP2):c.1080T>C (p.Thr360=)	ARMCX5-GPRASP2, GPRASP2	Single nucleotide variant (synonymous variant +1 more)	GPRASP2-related disorder +1 more	GBenign
Select item 2310947	NM_001004051.4(GPRASP2):c.1298C>T (p.Ala433Val)	ARMCX5-GPRASP2, GPRASP2 (A433V)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3033083	NM_001004051.4(GPRASP2):c.1509T>C (p.Phe503=)	ARMCX5-GPRASP2, GPRASP2	Single nucleotide variant (synonymous variant +1 more)	ARMCX5-GPRASP2-related disorder	GLikely benign
Select item 3040462	NM_001004051.4(GPRASP2):c.1636C>T (p.Pro546Ser)	ARMCX5-GPRASP2, GPRASP2 (P546S)	Single nucleotide variant (missense variant +1 more)	GPRASP2-related disorder	GLikely benign
Select item 780079	NM_001004051.4(GPRASP2):c.2163C>T (p.Ser721=)	ARMCX5-GPRASP2, GPRASP2	Single nucleotide variant (synonymous variant +1 more)	GPRASP2-related disorder +1 more	GBenign/Likely benign
Select item 3033681	NM_001004051.4(GPRASP2):c.2193T>C (p.Asn731=)	ARMCX5-GPRASP2, GPRASP2	Single nucleotide variant (synonymous variant +1 more)	GPRASP2-related disorder	GLikely benign
Select item 2661085	NM_001004051.4(GPRASP2):c.2484C>T (p.Asn828=)	ARMCX5-GPRASP2, GPRASP2	Single nucleotide variant (synonymous variant +1 more)	GPRASP2-related disorder +1 more	GLikely benign
Select item 3054389	NM_001004051.4(GPRASP2):c.*10C>A	ARMCX5-GPRASP2, GPRASP2	Single nucleotide variant (3 prime UTR variant +1 more)	GPRASP2-related disorder	GLikely benign