Related gene-specific medical variations for Gene (Select 2696) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3099899	NM_000164.4(GIPR):c.1231C>T (p.Arg411Cys)	GIPR, LOC130064721 (R375C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570306	NM_000164.4(GIPR):c.1210C>A (p.Arg404Ser)	GIPR, LOC130064721 (R368S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395527	NM_000164.4(GIPR):c.1244G>T (p.Ser415Ile)	GIPR, LOC130064721 (S379I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316499	NM_000164.4(GIPR):c.1339T>A (p.Ser447Thr)	GIPR, LOC130064721 (S447T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315293	NM_000164.4(GIPR):c.782T>A (p.Leu261His)	GIPR, LOC130064718 (L225H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287062	NM_000164.4(GIPR):c.1243A>G (p.Ser415Gly)	GIPR, LOC130064721 (S379G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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