C1868081[trait identifier] AND "Department of Molecular Diagnostics, I - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 617784	NM_004329.3(BMPR1A):c.176T>A (p.Leu59Ter)	BMPR1A (L59*)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 183728	NM_004329.3(BMPR1A):c.1081C>T (p.Arg361Ter)	BMPR1A (R361*)	Single nucleotide variant (nonsense)	Juvenile polyposis syndrome +4 more	GPathogenic