Related gene-specific medical variations for Gene (Select 84766) - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2626793	NM_001144958.2(CRACR2A):c.898G>T (p.Glu300Ter)	CRACR2A (E300*)	Single nucleotide variant (nonsense)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 2626792	NM_001144958.2(CRACR2A):c.430A>G (p.Arg144Gly)	CRACR2A	Single nucleotide variant (missense variant)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant

ClinVar