Related gene-specific medical variations for Gene (Select 7441) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3332136	NM_007128.4(VPREB1):c.13C>G (p.Pro5Ala)	IGL, VPREB1 (P5A)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3332135	NM_007128.4(VPREB1):c.80C>T (p.Pro27Leu)	IGL, VPREB1 (P26L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188735	NM_007128.4(VPREB1):c.67C>G (p.Leu23Val)	IGL, VPREB1 (L23V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188734	NM_007128.4(VPREB1):c.388G>C (p.Glu130Gln)	IGL, VPREB1 (E130Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188733	NM_007128.4(VPREB1):c.355G>T (p.Ala119Ser)	IGL, VPREB1 (A118S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188732	NM_007128.4(VPREB1):c.305T>A (p.Ile102Asn)	IGL, VPREB1 (I102N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188731	NM_007128.4(VPREB1):c.160G>A (p.Val54Ile)	IGL, VPREB1 (V54I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2531931	NM_007128.4(VPREB1):c.253C>T (p.Pro85Ser)	IGL, VPREB1 (P85S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470483	NM_007128.4(VPREB1):c.367G>C (p.Glu123Gln)	IGL, VPREB1 (E123Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379134	NM_007128.4(VPREB1):c.427C>T (p.Arg143Cys)	IGL, VPREB1 (R142C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358037	NM_007128.4(VPREB1):c.274G>A (p.Asp92Asn)	IGL, VPREB1 (D91N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205029	NM_007128.4(VPREB1):c.296A>T (p.Tyr99Phe)	IGL, VPREB1 (Y99F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance