Related gene-specific medical variations for Gene (Select 126861639) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2545981	NM_152591.3(CCDC63):c.90G>C (p.Glu30Asp)	CCDC63, LOC126861639 (E30D)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2455791	NM_152591.3(CCDC63):c.37G>T (p.Asp13Tyr)	CCDC63, LOC126861639 (D13Y)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance