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

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2390260	NM_024299.4(PPDPF):c.13C>T (p.Pro5Ser)	PPDPF (P5S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231301	NM_024299.4(PPDPF):c.40C>A (p.His14Asn)	PPDPF (H14N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620172	NM_024299.4(PPDPF):c.59G>A (p.Arg20His)	PPDPF (R20H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515516	NM_024299.4(PPDPF):c.59G>T (p.Arg20Leu)	PPDPF (R20L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3217056	NM_024299.4(PPDPF):c.139C>T (p.Pro47Ser)	PPDPF (P47S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3217057	NM_024299.4(PPDPF):c.143A>G (p.Lys48Arg)	PPDPF (K48R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3309103	NM_024299.4(PPDPF):c.261G>T (p.Met87Ile)	PPDPF (M87I)	Single nucleotide variant (stop lost +2 more)	not specified	GUncertain significance
Select item 3217058	NM_024299.4(PPDPF):c.265G>C (p.Ala89Pro)	PPDPF (A89P)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2376977	NM_024299.4(PPDPF):c.278C>T (p.Ala93Val)	PPDPF (A93V)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2538360	NM_024299.4(PPDPF):c.281G>T (p.Arg94Leu)	PPDPF (R94L)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3217059	NM_024299.4(PPDPF):c.290C>G (p.Pro97Arg)	PPDPF (P97R)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3217060	NM_024299.4(PPDPF):c.317G>A (p.Ser106Asn)	PPDPF (S106N)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2353451	NM_024299.4(PPDPF):c.322G>C (p.Ala108Pro)	PPDPF (A108P)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2330303	NM_024299.4(PPDPF):c.323C>G (p.Ala108Gly)	PPDPF (A108G)	Single nucleotide variant (3 prime UTR variant +2 more)	not provided +1 more	GUncertain significance
Select item 3217061	NM_024299.4(PPDPF):c.334C>A (p.Pro112Thr)	PPDPF (P112T)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2342744	NM_024299.4(PPDPF):c.337C>T (p.Pro113Ser)	PPDPF (P113S)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance