"Ambry Genetics"[submitter] AND "VIPR2"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3332079	NM_003382.5(VIPR2):c.1292T>G (p.Leu431Arg)	VIPR2 (L415R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2360371	NM_003382.5(VIPR2):c.1277G>T (p.Arg426Leu)	VIPR2 (R346L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379354	NM_003382.5(VIPR2):c.1268G>A (p.Arg423His)	VIPR2 (R407H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374220	NM_003382.5(VIPR2):c.1256T>C (p.Leu419Pro)	VIPR2 (L419P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3332082	NM_003382.5(VIPR2):c.1249G>C (p.Gly417Arg)	VIPR2 (G337R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188591	NM_003382.5(VIPR2):c.1239C>G (p.Asn413Lys)	VIPR2 (N397K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2305735	NM_003382.5(VIPR2):c.1226C>T (p.Ser409Phe)	VIPR2 (S393F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3332080	NM_003382.5(VIPR2):c.1223C>T (p.Ser408Phe)	VIPR2 (S408F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261100	NM_003382.5(VIPR2):c.1190C>A (p.Pro397Gln)	VIPR2 (P381Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2277241	NM_003382.5(VIPR2):c.1099C>A (p.Gln367Lys)	VIPR2 (Q367K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188598	NM_003382.5(VIPR2):c.983A>G (p.Lys328Arg)	VIPR2 (K312R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188597	NM_003382.5(VIPR2):c.941A>T (p.Asp314Val)	VIPR2 (D234V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325417	NM_003382.5(VIPR2):c.842G>C (p.Trp281Ser)	VIPR2 (W201S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314038	NM_003382.5(VIPR2):c.829C>T (p.His277Tyr)	VIPR2 (H197Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265323	NM_003382.5(VIPR2):c.808G>A (p.Gly270Ser)	VIPR2 (G270S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3332081	NM_003382.5(VIPR2):c.805A>T (p.Thr269Ser)	VIPR2 (T189S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3332078	NM_003382.5(VIPR2):c.790C>T (p.Leu264Phe)	VIPR2 (L184F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550250	NM_003382.5(VIPR2):c.790C>G (p.Leu264Val)	VIPR2 (L264V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188596	NM_003382.5(VIPR2):c.626T>C (p.Leu209Pro)	VIPR2 (L129P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487434	NM_003382.5(VIPR2):c.624C>G (p.Phe208Leu)	VIPR2 (F128L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529672	NM_003382.5(VIPR2):c.577C>T (p.Pro193Ser)	VIPR2 (P193S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3188594	NM_003382.5(VIPR2):c.448C>T (p.Leu150Phe)	LOC126860263, VIPR2 (L134F +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2330369	NM_003382.5(VIPR2):c.427A>G (p.Thr143Ala)	LOC126860263, VIPR2 (T127A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2527432	NM_003382.5(VIPR2):c.329G>A (p.Gly110Asp)	VIPR2 (G110D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477482	NM_003382.5(VIPR2):c.319G>A (p.Asp107Asn)	VIPR2 (D107N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342603	NM_003382.5(VIPR2):c.316G>A (p.Val106Ile)	VIPR2 (V106I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3188593	NM_003382.5(VIPR2):c.281C>T (p.Thr94Met)	VIPR2 (T94M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188592	NM_003382.5(VIPR2):c.215C>T (p.Thr72Met)	VIPR2 (T72M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2247975	NM_003382.5(VIPR2):c.160G>A (p.Gly54Ser)	VIPR2 (G54S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188595	NM_003382.5(VIPR2):c.61A>G (p.Ile21Val)	VIPR2 (I21V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 30