Related gene-specific medical variations for Gene (Select 389158) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3307868	NM_001085420.2(PLSCR5):c.728A>G (p.Asp243Gly)	PLSCR5, PLSCR5-AS1 (D231G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3307866	NM_001085420.2(PLSCR5):c.761G>A (p.Gly254Asp)	PLSCR5, PLSCR5-AS1 (G242D +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3215479	NM_001085420.2(PLSCR5):c.698C>T (p.Ala233Val)	PLSCR5, PLSCR5-AS1 (A233V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2522543	NM_001085420.2(PLSCR5):c.631G>C (p.Glu211Gln)	PLSCR5, PLSCR5-AS1 (E211Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347590	NM_001085420.2(PLSCR5):c.757A>G (p.Ile253Val)	PLSCR5, PLSCR5-AS1 (I253V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312177	NM_001085420.2(PLSCR5):c.733G>A (p.Asp245Asn)	PLSCR5, PLSCR5-AS1 (D245N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309811	NM_001085420.2(PLSCR5):c.737T>A (p.Val246Glu)	PLSCR5, PLSCR5-AS1 (V246E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar