Related gene-specific medical variations for Gene (Select 85462) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2363693	NM_001371116.1(FHDC1):c.1318A>G (p.Met440Val)	FHDC1, LOC126807195 (M440V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252416	NM_001371116.1(FHDC1):c.1370A>G (p.Asn457Ser)	FHDC1, LOC126807195 (N457S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 778161	NM_001371116.1(FHDC1):c.1260A>G (p.Gln420=)	FHDC1, LOC126807195	Single nucleotide variant (synonymous variant)	not provided	GBenign

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