"GeneKor MSA"[submitter] AND "RAD51B"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 584555	NM_133510.4(RAD51B):c.7A>G (p.Ser3Gly)	RAD51B (S3G)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 584553	NM_133510.4(RAD51B):c.25G>A (p.Val9Met)	RAD51B (V9M)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 221910	NM_133510.4(RAD51B):c.84G>A (p.Gln28=)	RAD51B	Single nucleotide variant (synonymous variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GLikely pathogenic
Select item 584552	NM_133510.4(RAD51B):c.226G>A (p.Ala76Thr)	RAD51B (A76T +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 584554	NM_133510.4(RAD51B):c.619G>T (p.Val207Leu)	RAD51B (V207L +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 584556	NM_133510.4(RAD51B):c.976C>G (p.Pro326Ala)	RAD51B (P326A +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 584557	NM_133510.4(RAD51B):c.983C>T (p.Ala328Val)	RAD51B (A328V +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 584550	NM_133510.4(RAD51B):c.1036+5G>A	RAD51B	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 584551	NM_133509.5(RAD51B):c.1063G>A (p.Ala355Thr)	RAD51B (A355T)	Single nucleotide variant (missense variant +1 more)	RAD51B-related disorder +2 more	GConflicting classifications of pathogenicity