"Ambry Genetics"[submitter] AND "GPRIN2"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282518	NM_001385282.1(GPRIN2):c.1325A>G (p.Gln442Arg)	GPRIN2 (Q442R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375033	NM_001385282.1(GPRIN2):c.1313G>A (p.Arg438Gln)	GPRIN2 (R462Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2203913	NM_001385282.1(GPRIN2):c.1312C>T (p.Arg438Trp)	GPRIN2 (R438W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282517	NM_001385282.1(GPRIN2):c.1297C>T (p.Arg433Trp)	GPRIN2 (R433W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345883	NM_001385282.1(GPRIN2):c.1259G>A (p.Arg420Gln)	GPRIN2 (R444Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211434	NM_001385282.1(GPRIN2):c.1202A>G (p.Glu401Gly)	GPRIN2 (E425G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525920	NM_001385282.1(GPRIN2):c.1135G>A (p.Val379Met)	GPRIN2 (V379M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491944	NM_001385282.1(GPRIN2):c.1055C>A (p.Pro352Gln)	GPRIN2 (P352Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367765	NM_001385282.1(GPRIN2):c.1055C>T (p.Pro352Leu)	GPRIN2 (P376L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282521	NM_001385282.1(GPRIN2):c.1051A>G (p.Ser351Gly)	GPRIN2 (S375G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511129	NM_001385282.1(GPRIN2):c.1016C>T (p.Ala339Val)	GPRIN2 (A363V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3102024	NM_001385282.1(GPRIN2):c.929C>A (p.Thr310Asn)	GPRIN2 (T310N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610000	NM_001385282.1(GPRIN2):c.922T>C (p.Ser308Pro)	GPRIN2 (S332P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380779	NM_001385282.1(GPRIN2):c.881C>T (p.Ala294Val)	GPRIN2 (A318V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547116	NM_001385282.1(GPRIN2):c.700C>A (p.Leu234Ile)	GPRIN2 (L258I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282519	NM_001385282.1(GPRIN2):c.688C>T (p.Pro230Ser)	GPRIN2 (P254S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2559080	NM_001385282.1(GPRIN2):c.655G>A (p.Glu219Lys)	GPRIN2 (E219K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476704	NM_001385282.1(GPRIN2):c.653C>T (p.Ala218Val)	GPRIN2 (A218V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102023	NM_001385282.1(GPRIN2):c.571G>A (p.Ala191Thr)	GPRIN2 (A191T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282522	NM_001385282.1(GPRIN2):c.505C>A (p.Pro169Thr)	GPRIN2 (P193T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495434	NM_001385282.1(GPRIN2):c.388A>T (p.Met130Leu)	GPRIN2 (M130L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282520	NM_001385282.1(GPRIN2):c.331G>C (p.Ala111Pro)	GPRIN2 (A135P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288682	NM_001385282.1(GPRIN2):c.305G>A (p.Gly102Asp)	GPRIN2 (G102D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102022	NM_001385282.1(GPRIN2):c.185C>T (p.Pro62Leu)	GPRIN2 (P86L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3102025	NM_001385282.1(GPRIN2):c.97C>T (p.Arg33Trp)	GPRIN2 (R33W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25