POP5[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 2603448	NM_015918.4(POP5):c.484A>G (p.Met162Val)	POP5 (M162V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216785	NM_015918.4(POP5):c.416A>G (p.Gln139Arg)	POP5 (Q139R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308920	NM_015918.4(POP5):c.384C>G (p.Asn128Lys)	POP5 (N78K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308922	NM_015918.4(POP5):c.359G>A (p.Arg120Lys)	POP5 (R70K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456332	NM_015918.4(POP5):c.277C>A (p.Arg93Ser)	POP5 (R93S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532622	NM_015918.4(POP5):c.211A>G (p.Lys71Glu)	POP5 (K71E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456232	NM_015918.4(POP5):c.117G>T (p.Arg39Ser)	POP5 (R39S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528502	NM_015918.4(POP5):c.59G>A (p.Cys20Tyr)	POP5 (C20Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216784	NM_015918.4(POP5):c.18C>G (p.His6Gln)	POP5 (H6Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance