Related gene-specific medical variations for Gene (Select 101927418) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2398402	NM_001017923.2(C14orf28):c.443C>T (p.Ser148Phe)	C14orf28, LOC101927418 (S148F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229588	NM_001017923.2(C14orf28):c.844C>T (p.Leu282Phe)	C14orf28, LOC101927418 (L282F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 789639	NM_001017923.2(C14orf28):c.927G>T (p.Glu309Asp)	C14orf28, LOC101927418 (E309D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 785459	NM_001017923.2(C14orf28):c.198A>G (p.Leu66=)	C14orf28, LOC101927418	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 776833	NM_001017923.2(C14orf28):c.701C>T (p.Ser234Phe)	C14orf28, LOC101927418 (S234F)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 727384	NM_001017923.2(C14orf28):c.530C>T (p.Pro177Leu)	C14orf28, LOC101927418 (P177L)	Single nucleotide variant (missense variant)	not provided	GBenign

ClinVar