FXYD5[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3097576	NM_014164.6(FXYD5):c.68C>T (p.Thr23Met)	FXYD5 (T23M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341034	NM_014164.6(FXYD5):c.134G>A (p.Arg45Gln)	FXYD5 (R45Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 91979	NM_014164.6(FXYD5):c.280A>G (p.Ser94Gly)	FXYD5 (S94G)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2552088	NM_014164.6(FXYD5):c.310A>C (p.Thr104Pro)	FXYD5 (T73P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097574	NM_014164.6(FXYD5):c.338C>T (p.Pro113Leu)	FXYD5 (P113L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352209	NM_014164.6(FXYD5):c.361C>T (p.Pro121Ser)	FXYD5 (P90S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219046	NM_014164.6(FXYD5):c.418C>T (p.His140Tyr)	FXYD5 (H140Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398167	NM_014164.6(FXYD5):c.427C>T (p.Arg143Trp)	FXYD5 (R112W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210377	NM_014164.6(FXYD5):c.512G>A (p.Arg171Gln)	FXYD5 (R140Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign