CLDND1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2389591	NM_001040181.2(CLDND1):c.628G>A (p.Gly210Ser)	CLDND1 (G210S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2540903	NM_001040181.2(CLDND1):c.602A>G (p.Lys201Arg)	CLDND1 (K106R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2536827	NM_001040181.2(CLDND1):c.436G>A (p.Val146Met)	CLDND1 (V51M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493902	NM_001040181.2(CLDND1):c.346A>T (p.Met116Leu)	CLDND1 (M116L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2281722	NM_001040181.2(CLDND1):c.256A>G (p.Lys86Glu)	CLDND1 (K109E +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2310961	NM_001040181.2(CLDND1):c.212A>G (p.Tyr71Cys)	CLDND1 (Y94C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2330574	NM_001040181.2(CLDND1):c.196G>A (p.Asp66Asn)	CLDND1 (D89N +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2615723	NM_001040181.2(CLDND1):c.188C>A (p.Thr63Asn)	CLDND1 (T63N +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2398943	NM_001040181.2(CLDND1):c.146G>C (p.Ser49Thr)	CLDND1 (S49T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2557716	NM_001040181.2(CLDND1):c.79A>G (p.Ile27Val)	CLDND1 (I27V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2361318	NM_001040181.2(CLDND1):c.74C>T (p.Ala25Val)	CLDND1 (A25V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance