"PreventionGenetics, part of Exact Sciences"[submitter] AND "MAD2L2"[g - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2180851	NM_006341.4(MAD2L2):c.618C>T (p.Arg206=)	MAD2L2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 731771	NM_006341.4(MAD2L2):c.606C>T (p.Tyr202=)	MAD2L2	Single nucleotide variant (synonymous variant)	MAD2L2-related disorder +1 more	GBenign/Likely benign
Select item 726312	NM_006341.4(MAD2L2):c.582G>A (p.Ser194=)	MAD2L2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 767652	NM_006341.4(MAD2L2):c.399C>T (p.Cys133=)	MAD2L2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2900744	NM_006341.4(MAD2L2):c.393C>T (p.Ser131=)	MAD2L2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2146960	NM_006341.4(MAD2L2):c.354T>C (p.His118=)	MAD2L2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2634658	NM_006341.4(MAD2L2):c.338A>C (p.Asp113Ala)	MAD2L2 (D113A)	Single nucleotide variant (missense variant)	MAD2L2-related disorder	GUncertain significance
Select item 743486	NM_006341.4(MAD2L2):c.278G>A (p.Arg93His)	MAD2L2 (R93H)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2628926	NM_006341.4(MAD2L2):c.200C>T (p.Thr67Met)	MAD2L2 (T67M)	Single nucleotide variant (missense variant)	MAD2L2-related disorder	GUncertain significance
Select item 2070063	NM_006341.4(MAD2L2):c.114C>T (p.Pro38=)	MAD2L2	Single nucleotide variant (synonymous variant)	MAD2L2-related disorder +1 more	GLikely benign
Select item 775512	NM_006341.4(MAD2L2):c.41-7C>A	LOC129929411, MAD2L2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign