"Ambry Genetics"[submitter] AND "GPR45"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2177107	NM_007227.3(GPR45):c.17C>T (p.Thr6Met)	GPR45 (T6M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1898558	NM_007227.3(GPR45):c.37T>C (p.Tyr13His)	GPR45 (Y13H)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2384491	NM_007227.3(GPR45):c.119T>C (p.Val40Ala)	GPR45 (V40A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2428083	NM_007227.3(GPR45):c.194T>C (p.Met65Thr)	GPR45 (M65T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1438315	NM_007227.3(GPR45):c.229G>T (p.Ala77Ser)	GPR45 (A77S)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1990839	NM_007227.3(GPR45):c.325C>T (p.Leu109Phe)	GPR45 (L109F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2615794	NM_007227.3(GPR45):c.466T>C (p.Trp156Arg)	GPR45 (W156R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2860957	NM_007227.3(GPR45):c.535G>A (p.Ala179Thr)	GPR45 (A179T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1433709	NM_007227.3(GPR45):c.675C>G (p.Asn225Lys)	GPR45 (N225K)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1420542	NM_007227.3(GPR45):c.751C>T (p.Arg251Trp)	GPR45 (R251W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance