"PreventionGenetics, part of Exact Sciences"[submitter] AND "GPR174"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042309	NM_032553.3(GPR174):c.222G>A (p.Leu74=)	GPR174	Single nucleotide variant (synonymous variant)	GPR174-related disorder	GLikely benign
Select item 3041228	NM_032553.3(GPR174):c.263C>A (p.Pro88His)	GPR174 (P88H)	Single nucleotide variant (missense variant)	GPR174-related disorder	GLikely benign
Select item 753511	NM_032553.3(GPR174):c.423C>T (p.Gly141=)	GPR174	Single nucleotide variant (synonymous variant)	GPR174-related disorder +1 more	GLikely benign
Select item 708865	NM_032553.3(GPR174):c.483C>T (p.Thr161=)	GPR174	Single nucleotide variant (synonymous variant)	GPR174-related disorder +1 more	GBenign
Select item 3058904	NM_032553.3(GPR174):c.484T>C (p.Ser162Pro)	GPR174 (S162P)	Single nucleotide variant (missense variant)	GPR174-related disorder	GBenign
Select item 3029517	NM_032553.3(GPR174):c.546C>T (p.Ser182=)	GPR174	Single nucleotide variant (synonymous variant)	GPR174-related disorder	GLikely benign
Select item 3042805	NM_032553.3(GPR174):c.606A>G (p.Leu202=)	GPR174	Single nucleotide variant (synonymous variant)	GPR174-related disorder	GBenign

ClinVar