"PreventionGenetics, part of Exact Sciences"[submitter] AND "CAD"[gene - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 729628	NM_004341.5(CAD):c.686A>G (p.Tyr229Cys)	CAD (Y229C)	Single nucleotide variant (missense variant)	CAD-related disorder +2 more	GLikely benign
Select item 720046	NM_004341.5(CAD):c.713G>A (p.Arg238His)	CAD (R238H)	Single nucleotide variant (missense variant)	CAD-related disorder +1 more	GLikely benign
Select item 2789919	NM_004341.5(CAD):c.820C>A (p.Arg274=)	CAD	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GLikely benign
Select item 1582314	NM_004341.5(CAD):c.995+10G>A	CAD	Single nucleotide variant (intron variant)	CAD-related disorder +1 more	GLikely benign
Select item 714610	NM_004341.5(CAD):c.1083A>G (p.Thr361=)	CAD	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GBenign/Likely benign
Select item 712897	NM_004341.5(CAD):c.1109-4A>G	CAD	Single nucleotide variant (intron variant)	CAD-related disorder +1 more	GBenign/Likely benign
Select item 726316	NM_004341.5(CAD):c.1158C>T (p.Pro386=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1653081	NM_004341.5(CAD):c.1203A>G (p.Ser401=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3058355	NM_004341.5(CAD):c.1503C>T (p.Val501=)	CAD	Single nucleotide variant (synonymous variant)	CAD-related disorder	GLikely benign
Select item 2630121	NM_004341.5(CAD):c.1540G>A (p.Asp514Asn)	CAD (D514N)	Single nucleotide variant (missense variant)	CAD-related disorder	GUncertain significance
Select item 732083	NM_004341.5(CAD):c.1632C>T (p.Ala544=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1638720	NM_004341.5(CAD):c.1917A>C (p.Thr639=)	CAD	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1572290	NM_004341.5(CAD):c.2032-8C>T	CAD	Single nucleotide variant (intron variant)	CAD-related disorder +1 more	GLikely benign
Select item 788389	NM_004341.5(CAD):c.2079G>A (p.Leu693=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 779864	NM_004341.5(CAD):c.2576C>T (p.Pro859Leu)	CAD, LOC126806171 (P859L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 793341	NM_004341.5(CAD):c.2577G>A (p.Pro859=)	CAD, LOC126806171	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GBenign/Likely benign
Select item 2775490	NM_004341.5(CAD):c.2646-3dup	CAD, LOC126806171	Duplication (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 755748	NM_004341.5(CAD):c.2868A>G (p.Val956=)	CAD, LOC126806171	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GLikely benign
Select item 1571652	NM_004341.5(CAD):c.2886C>G (p.Leu962=)	CAD	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GLikely benign
Select item 1953349	NM_004341.5(CAD):c.3015C>T (p.Leu1005=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 710412	NM_004341.5(CAD):c.3162C>T (p.Leu1054=)	CAD	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GBenign/Likely benign
Select item 1624427	NM_004341.5(CAD):c.3348C>T (p.Ala1116=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 745045	NM_004341.5(CAD):c.3400-7C>T	CAD	Single nucleotide variant (intron variant)	CAD-related disorder +1 more	GBenign/Likely benign
Select item 1916175	NM_004341.5(CAD):c.3438G>T (p.Val1146=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1614054	NM_004341.5(CAD):c.3510C>T (p.Pro1170=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 789878	NM_004341.5(CAD):c.3975A>G (p.Lys1325=)	CAD	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GBenign/Likely benign
Select item 1079072	NM_004341.5(CAD):c.4320A>G (p.Leu1440=)	CAD	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GLikely benign
Select item 786478	NM_004341.5(CAD):c.4596G>A (p.Ala1532=)	CAD	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GBenign/Likely benign
Select item 1556334	NM_004341.5(CAD):c.4599A>G (p.Leu1533=)	CAD	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GLikely benign
Select item 1597364	NM_004341.5(CAD):c.4785C>T (p.Thr1595=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1532655	NM_004341.5(CAD):c.4786G>A (p.Val1596Met)	CAD (V1533M +1 more)	Single nucleotide variant (missense variant)	CAD-related disorder +2 more	GLikely benign
Select item 1625486	NM_004341.5(CAD):c.4929G>T (p.Leu1643=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 788724	NM_004341.5(CAD):c.4930T>C (p.Phe1644Leu)	CAD (F1581L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +4 more	GBenign/Likely benign
Select item 1411932	NM_004341.5(CAD):c.5060A>G (p.His1687Arg)	CAD (H1624R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1638125	NM_004341.5(CAD):c.5352C>T (p.Arg1784=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1596968	NM_004341.5(CAD):c.5382T>C (p.Tyr1794=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3055263	NM_004341.5(CAD):c.5639-4G>A	CAD	Single nucleotide variant (intron variant)	CAD-related disorder	GLikely benign
Select item 736022	NM_004341.5(CAD):c.5979C>T (p.Ser1993=)	CAD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 808715	NM_004341.5(CAD):c.6001G>A (p.Val2001Ile)	CAD (V1938I +1 more)	Single nucleotide variant (missense variant)	CAD-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 377271	NM_004341.5(CAD):c.6343G>C (p.Val2115Leu)	CAD, LOC126806172 (V2115L +1 more)	Single nucleotide variant (missense variant)	CAD-related disorder +1 more	GBenign/Likely benign
Select item 1281984	NM_004341.5(CAD):c.6660C>T (p.Thr2220=)	LOC126806172, CAD	Single nucleotide variant (synonymous variant)	CAD-related disorder +1 more	GBenign

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Items: 41