Related gene-specific medical variations for Gene (Select 30819) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3113298	NM_173191.3(KCNIP2):c.598G>A (p.Glu200Lys)	KCNIP2, KCNIP2-AS1 +1 more (E157K +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542429	NM_173191.3(KCNIP2):c.426C>G (p.Ser142Arg)	KCNIP2, KCNIP2-AS1 +1 more (S157R +5 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2516245	NM_173191.3(KCNIP2):c.662G>A (p.Arg221Gln)	KCNIP2, KCNIP2-AS1 +1 more (R176Q +6 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2512745	NM_173191.3(KCNIP2):c.706A>G (p.Met236Val)	KCNIP2, KCNIP2-AS1 +1 more (M150V +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337417	NM_173191.3(KCNIP2):c.763A>C (p.Lys255Gln)	KCNIP2, KCNIP2-AS1 +1 more (K210Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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