"Ambry Genetics"[submitter] AND "ADAMDEC1"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2530027	NM_014479.3(ADAMDEC1):c.32T>C (p.Val11Ala)	ADAM7-AS1, ADAMDEC1 (V11A)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2329796	NM_014479.3(ADAMDEC1):c.34G>A (p.Ala12Thr)	ADAMDEC1, ADAM7-AS1 (A12T)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2542206	NM_014479.3(ADAMDEC1):c.131T>C (p.Ile44Thr)	ADAM7-AS1, ADAMDEC1 (I44T)	Single nucleotide variant (5 prime UTR variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2483668	NM_014479.3(ADAMDEC1):c.188C>T (p.Thr63Ile)	ADAM7-AS1, ADAMDEC1 (T63I)	Single nucleotide variant (5 prime UTR variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2560021	NM_014479.3(ADAMDEC1):c.199G>A (p.Gly67Ser)	ADAM7-AS1, ADAMDEC1 (G67S)	Single nucleotide variant (5 prime UTR variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2387390	NM_014479.3(ADAMDEC1):c.286C>A (p.His96Asn)	ADAMDEC1, ADAM7-AS1 (H17N +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2359560	NM_014479.3(ADAMDEC1):c.421A>G (p.Ser141Gly)	ADAM7-AS1, ADAMDEC1 (S62G +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2546140	NM_014479.3(ADAMDEC1):c.433G>A (p.Gly145Arg)	ADAM7-AS1, ADAMDEC1 (G145R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2289304	NM_014479.3(ADAMDEC1):c.512C>A (p.Ala171Asp)	ADAMDEC1, ADAM7-AS1 (A171D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2589363	NM_014479.3(ADAMDEC1):c.514G>T (p.Val172Phe)	ADAM7-AS1, ADAMDEC1 (V172F +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2220605	NM_014479.3(ADAMDEC1):c.554A>G (p.His185Arg)	ADAM7-AS1, ADAMDEC1 (H106R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2461761	NM_014479.3(ADAMDEC1):c.580G>A (p.Gly194Arg)	ADAM7-AS1, ADAMDEC1 (G194R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2532316	NM_014479.3(ADAMDEC1):c.643C>T (p.Arg215Trp)	ADAM7-AS1, ADAMDEC1 (R136W +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2319443	NM_014479.3(ADAMDEC1):c.746T>C (p.Met249Thr)	ADAM7-AS1, ADAMDEC1 (M170T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2558339	NM_014479.3(ADAMDEC1):c.833A>G (p.Lys278Arg)	ADAM7-AS1, ADAMDEC1 (K278R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2259932	NM_014479.3(ADAMDEC1):c.1097A>T (p.Asn366Ile)	ADAM7-AS1, ADAMDEC1 (N366I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2322119	NM_014479.3(ADAMDEC1):c.1194A>C (p.Arg398Ser)	ADAMDEC1, ADAM7-AS1 (R398S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2568606	NM_014479.3(ADAMDEC1):c.1274A>T (p.Asn425Ile)	ADAM7-AS1, ADAMDEC1 (N346I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2528561	NM_014479.3(ADAMDEC1):c.1384G>A (p.Gly462Arg)	ADAM7-AS1, ADAMDEC1 (G383R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance