Related gene-specific medical variations for Gene (Select 55421) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3298748	NM_001114118.3(NCBP3):c.7G>A (p.Ala3Thr)	LOC130059992, NCBP3 (A3T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181858	NM_001114118.3(NCBP3):c.92G>C (p.Gly31Ala)	LOC130059992, NCBP3 (G31A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181833	NM_001114118.3(NCBP3):c.62T>C (p.Leu21Pro)	LOC130059992, NCBP3 (L21P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473586	NM_001114118.3(NCBP3):c.38C>T (p.Ala13Val)	LOC130059992, NCBP3 (A13V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470183	NM_001114118.3(NCBP3):c.180C>G (p.Ile60Met)	LOC130059992, NCBP3 (I60M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467804	NM_001114118.3(NCBP3):c.110C>T (p.Pro37Leu)	LOC130059992, NCBP3 (P37L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388128	NM_001114118.3(NCBP3):c.22C>T (p.Arg8Trp)	LOC130059992, NCBP3 (R8W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386632	NM_001114118.3(NCBP3):c.157C>T (p.Arg53Trp)	LOC130059992, NCBP3 (R53W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353116	NM_001114118.3(NCBP3):c.44C>T (p.Ala15Val)	LOC130059992, NCBP3 (A15V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305942	NM_001114118.3(NCBP3):c.164C>T (p.Ser55Leu)	LOC130059992, NCBP3 (S55L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance