"PreventionGenetics, part of Exact Sciences"[submitter] AND "GPR180"[g - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042434	NM_180989.6(GPR180):c.145+9G>C	GPR180, LOC121468002	Single nucleotide variant (intron variant)	GPR180-related disorder	GLikely benign
Select item 3052985	NM_180989.6(GPR180):c.321C>T (p.Thr107=)	GPR180	Single nucleotide variant (synonymous variant)	GPR180-related disorder	GLikely benign
Select item 3059123	NM_180989.6(GPR180):c.459A>G (p.Pro153=)	GPR180	Single nucleotide variant (synonymous variant)	GPR180-related disorder	GBenign
Select item 3060414	NM_180989.6(GPR180):c.465C>T (p.Ala155=)	GPR180	Single nucleotide variant (synonymous variant)	GPR180-related disorder	GBenign
Select item 3047227	NM_180989.6(GPR180):c.574T>C (p.Leu192=)	GPR180	Single nucleotide variant (synonymous variant)	GPR180-related disorder	GLikely benign
Select item 3033861	NM_180989.6(GPR180):c.813G>C (p.Met271Ile)	GPR180 (M271I)	Single nucleotide variant (missense variant)	GPR180-related disorder	GBenign
Select item 3059754	NM_180989.6(GPR180):c.852G>A (p.Thr284=)	GPR180	Single nucleotide variant (synonymous variant)	GPR180-related disorder	GBenign
Select item 3038153	NM_180989.6(GPR180):c.926A>G (p.Asp309Gly)	GPR180 (D309G)	Single nucleotide variant (missense variant)	GPR180-related disorder	GBenign
Select item 3050358	NM_180989.6(GPR180):c.1049G>A (p.Ser350Asn)	GPR180 (S350N)	Single nucleotide variant (missense variant)	GPR180-related disorder	GBenign
Select item 3034012	NM_180989.6(GPR180):c.1155A>G (p.Gln385=)	GPR180	Single nucleotide variant (synonymous variant)	GPR180-related disorder	GLikely benign