"PreventionGenetics, part of Exact Sciences"[submitter] AND "DECR1"[ge - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 534666	NM_001359.2(DECR1):c.77G>A (p.Ser26Asn)	DECR1 (S26N +1 more)	Single nucleotide variant (missense variant)	DECR1-related disorder +1 more	GBenign/Likely benign
Select item 3040772	NM_001359.2(DECR1):c.258C>T (p.Cys86=)	DECR1	Single nucleotide variant (synonymous variant)	DECR1-related disorder	GLikely benign
Select item 3056853	NM_001359.2(DECR1):c.860A>G (p.Asp287Gly)	DECR1 (D278G +1 more)	Single nucleotide variant (missense variant)	DECR1-related disorder	GLikely benign

Format

Sort by

Choose Destination

ClinVar