"Ambry Genetics"[submitter] AND "GRAP2"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3102205	NM_004810.4(GRAP2):c.38G>A (p.Gly13Asp)	GRAP2 (G13D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3282608	NM_004810.4(GRAP2):c.110C>T (p.Ala37Val)	GRAP2 (A37V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102202	NM_004810.4(GRAP2):c.139C>A (p.Pro47Thr)	GRAP2 (P47T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282610	NM_004810.4(GRAP2):c.271G>T (p.Asp91Tyr)	GRAP2 (D19Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102203	NM_004810.4(GRAP2):c.273C>A (p.Asp91Glu)	GRAP2 (D91E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102204	NM_004810.4(GRAP2):c.326G>A (p.Arg109Gln)	GRAP2 (R37Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488110	NM_004810.4(GRAP2):c.428T>C (p.Ile143Thr)	GRAP2 (I143T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455439	NM_004810.4(GRAP2):c.446C>A (p.Thr149Asn)	GRAP2 (T149N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395337	NM_004810.4(GRAP2):c.449G>A (p.Arg150Gln)	GRAP2 (R150Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512268	NM_004810.4(GRAP2):c.484C>T (p.Arg162Trp)	GRAP2 (R162W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597187	NM_004810.4(GRAP2):c.551G>A (p.Arg184Gln)	GRAP2 (R112Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392991	NM_004810.4(GRAP2):c.574A>C (p.Thr192Pro)	GRAP2 (T192P +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3102206	NM_004810.4(GRAP2):c.675C>G (p.His225Gln)	GRAP2 (H112Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568867	NM_004810.4(GRAP2):c.715A>G (p.Ile239Val)	GRAP2 (I167V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102207	NM_004810.4(GRAP2):c.770T>A (p.Met257Lys)	GRAP2 (M144K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252687	NM_004810.4(GRAP2):c.830G>A (p.Arg277Gln)	GRAP2 (R277Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358118	NM_004810.4(GRAP2):c.934C>T (p.Arg312Cys)	GRAP2 (R199C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance