Related gene-specific medical variations for Gene (Select 27299) - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3266328	NM_014479.3(ADAMDEC1):c.881A>G (p.His294Arg)	ADAM7-AS1, ADAMDEC1 (H215R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3266322	NM_014479.3(ADAMDEC1):c.487A>G (p.Lys163Glu)	ADAM7-AS1, ADAMDEC1 (K163E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3266317	NM_014479.3(ADAMDEC1):c.11G>A (p.Gly4Glu)	ADAM7-AS1, ADAMDEC1 (G4E)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3266308	NM_014479.3(ADAMDEC1):c.1381G>A (p.Gly461Arg)	ADAM7-AS1, ADAMDEC1 (G382R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3146434	NM_014479.3(ADAMDEC1):c.962T>C (p.Leu321Pro)	ADAM7-AS1, ADAMDEC1 (L321P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3146432	NM_014479.3(ADAMDEC1):c.911A>G (p.Asp304Gly)	ADAM7-AS1, ADAMDEC1 (D225G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3146422	NM_014479.3(ADAMDEC1):c.733G>A (p.Val245Met)	ADAM7-AS1, ADAMDEC1 (V245M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3146409	NM_014479.3(ADAMDEC1):c.575C>T (p.Thr192Ile)	ADAM7-AS1, ADAMDEC1 (T113I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3146400	NM_014479.3(ADAMDEC1):c.505G>A (p.Glu169Lys)	ADAM7-AS1, ADAMDEC1 (E169K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3146385	NM_014479.3(ADAMDEC1):c.317T>C (p.Leu106Ser)	ADAM7-AS1, ADAMDEC1 (L106S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3146369	NM_014479.3(ADAMDEC1):c.1373C>A (p.Thr458Asn)	ADAM7-AS1, ADAMDEC1 (T458N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3146361	NM_014479.3(ADAMDEC1):c.1277A>G (p.His426Arg)	ADAM7-AS1, ADAMDEC1 (H347R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	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)	not specified	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)	not specified	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)	not specified	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)	not specified	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)	not specified	GUncertain significance
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)	not specified	GUncertain significance
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)	not specified	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)	not specified	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)	not specified	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)	not specified	GLikely benign
Select item 2387390	NM_014479.3(ADAMDEC1):c.286C>A (p.His96Asn)	ADAM7-AS1, ADAMDEC1 (H17N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	GUncertain significance
Select item 2329796	NM_014479.3(ADAMDEC1):c.34G>A (p.Ala12Thr)	ADAM7-AS1, ADAMDEC1 (A12T)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2322119	NM_014479.3(ADAMDEC1):c.1194A>C (p.Arg398Ser)	ADAM7-AS1, ADAMDEC1 (R398S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	GUncertain significance
Select item 2289304	NM_014479.3(ADAMDEC1):c.512C>A (p.Ala171Asp)	ADAM7-AS1, ADAMDEC1 (A171D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	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)	not specified	GUncertain significance
Select item 786556	NM_014479.3(ADAMDEC1):c.119C>T (p.Thr40Met)	ADAM7-AS1, ADAMDEC1 (T40M)	Single nucleotide variant (5 prime UTR variant +3 more)	not provided	GBenign
Select item 782511	NM_014479.3(ADAMDEC1):c.762+10T>C	ADAM7-AS1, ADAMDEC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 781137	NM_014479.3(ADAMDEC1):c.1323G>A (p.Glu441=)	ADAM7-AS1, ADAMDEC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 781136	NM_014479.3(ADAMDEC1):c.1315C>T (p.Pro439Ser)	ADAM7-AS1, ADAMDEC1 (P439S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 781135	NM_014479.3(ADAMDEC1):c.888T>C (p.Ser296=)	ADAMDEC1, ADAM7-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 781134	NM_014479.3(ADAMDEC1):c.765A>T (p.Ile255=)	ADAM7-AS1, ADAMDEC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 781121	NM_014479.3(ADAMDEC1):c.362T>C (p.Met121Thr)	ADAM7-AS1, ADAMDEC1 (M121T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 781120	NM_014479.3(ADAMDEC1):c.242T>C (p.Ile81Thr)	ADAM7-AS1, ADAMDEC1 (I81T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 717905	NM_014479.3(ADAMDEC1):c.131T>G (p.Ile44Arg)	ADAMDEC1, ADAM7-AS1 (I44R)	Single nucleotide variant (5 prime UTR variant +3 more)	not provided	GBenign

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Links from Gene

Items: 40