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

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2241694	NM_000164.4(GIPR):c.22C>G (p.Gln8Glu)	GIPR (Q8E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099901	NM_000164.4(GIPR):c.34C>G (p.Arg12Gly)	GIPR (R12G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456855	NM_000164.4(GIPR):c.47G>A (p.Cys16Tyr)	GIPR (C16Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492131	NM_000164.4(GIPR):c.49G>A (p.Gly17Arg)	GIPR (G17R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339550	NM_000164.4(GIPR):c.68C>G (p.Ala23Gly)	GIPR (A23G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230467	NM_000164.4(GIPR):c.92C>A (p.Thr31Lys)	GIPR (T31K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249497	NM_000164.4(GIPR):c.101A>G (p.Glu34Gly)	GIPR (E34G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099898	NM_000164.4(GIPR):c.107A>C (p.Tyr36Ser)	GIPR (Y36S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099900	NM_000164.4(GIPR):c.197A>T (p.Asp66Val)	GIPR (D66V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328772	NM_000164.4(GIPR):c.331C>G (p.Leu111Val)	GIPR (L111V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228395	NM_000164.4(GIPR):c.387C>A (p.Asp129Glu)	GIPR (D129E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342620	NM_000164.4(GIPR):c.419T>C (p.Met140Thr)	GIPR (M104T +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 2239278	NM_000164.4(GIPR):c.856T>C (p.Cys286Arg)	GIPR (C286R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285719	NM_000164.4(GIPR):c.898C>T (p.Arg300Trp)	GIPR (R264W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374277	NM_000164.4(GIPR):c.911T>G (p.Leu304Arg)	GIPR (L268R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099902	NM_000164.4(GIPR):c.913A>G (p.Met305Val)	GIPR (M305V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286021	NM_000164.4(GIPR):c.1067T>C (p.Val356Ala)	GIPR (V356A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402762	NM_000164.4(GIPR):c.1108C>A (p.Arg370Ser)	GIPR (R370S +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 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 2287062	NM_000164.4(GIPR):c.1243A>G (p.Ser415Gly)	GIPR, LOC130064721 (S379G +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

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Items: 24