"RAD51-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2636942	NM_002875.5(RAD51):c.53_69delinsTATCTTCTT (p.Glu18fs)	RAD51 (E18fs)	Indel (frameshift variant)	RAD51-related disorder	GLikely pathogenic
Select item 743937	NM_002875.5(RAD51):c.144T>C (p.Thr48=)	RAD51	Single nucleotide variant (synonymous variant)	RAD51-related disorder +2 more	GLikely benign
Select item 1777453	NM_002875.5(RAD51):c.165G>A (p.Ala55=)	RAD51	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 1777870	NM_002875.5(RAD51):c.167C>T (p.Pro56Leu)	RAD51 (P56L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3043549	NM_002875.5(RAD51):c.225+599_225+601del	RAD51	Deletion (intron variant)	RAD51-related disorder	GLikely benign
Select item 3042565	NM_002875.5(RAD51):c.225+601del	RAD51	Deletion (intron variant)	RAD51-related disorder	GLikely benign
Select item 1197702	NM_002875.5(RAD51):c.225+600_225+601del	RAD51	Deletion (intron variant)	not provided +1 more	GLikely benign
Select item 3041826	NM_002875.5(RAD51):c.225+716G>A	RAD51 (G113R)	Single nucleotide variant (missense variant +1 more)	RAD51-related disorder	GLikely benign
Select item 3030530	NM_002875.5(RAD51):c.344-3dup	RAD51	Duplication (intron variant)	RAD51-related disorder	GLikely benign
Select item 3033883	NM_002875.5(RAD51):c.435+8G>A	RAD51	Single nucleotide variant (intron variant)	RAD51-related disorder	GLikely benign
Select item 13127	NM_002875.5(RAD51):c.449G>A (p.Arg150Gln)	RAD51 (R150Q +1 more)	Single nucleotide variant (missense variant)	RAD51-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 1743081	NM_002875.5(RAD51):c.478A>G (p.Ile160Val)	RAD51 (I160V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2072406	NM_002875.5(RAD51):c.671C>G (p.Ala224Gly)	RAD51 (A224G +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 751562	NM_002875.5(RAD51):c.675C>T (p.Thr225=)	RAD51	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 718568	NM_002875.5(RAD51):c.720C>G (p.Ala240=)	RAD51	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 372139	NM_002875.5(RAD51):c.877G>A (p.Ala293Thr)	RAD51 (A293T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GPathogenic/Likely pathogenic
Select item 1337171	NM_002875.5(RAD51):c.885A>G (p.Ala295=)	RAD51	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +3 more	GLikely benign
Select item 722625	NM_002875.5(RAD51):c.945C>T (p.Tyr315=)	RAD51 (R275*)	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign