"Pathway Genomics"[submitter] AND "BRIP1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 128175	NM_032043.3(BRIP1):c.2564G>A (p.Arg855His)	BRIP1 (R855H)	Single nucleotide variant (missense variant)	BRIP1-related condition +6 more	GUncertain significance
Select item 156494	NM_032043.3(BRIP1):c.2364T>A (p.Asn788Lys)	BRIP1 (N788K)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group J	GUncertain significance