Related gene-specific medical variations for Gene (Select 114787) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2656094	NM_052899.3(GPRIN1):c.2595C>T (p.Ala865=)	GPRIN1, LOC129995349	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2614970	NM_052899.3(GPRIN1):c.2920G>A (p.Ala974Thr)	GPRIN1, LOC129995348 (A974T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387967	NM_052899.3(GPRIN1):c.2603C>A (p.Thr868Lys)	GPRIN1, LOC129995349 (T868K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324350	NM_052899.3(GPRIN1):c.2591G>A (p.Gly864Asp)	GPRIN1, LOC129995349 (G864D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270655	NM_052899.3(GPRIN1):c.2639C>T (p.Ala880Val)	GPRIN1, LOC129995349 (A880V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228396	NM_052899.3(GPRIN1):c.2626A>G (p.Met876Val)	GPRIN1, LOC129995349 (M876V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar