"XRCC1-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040249	NM_006297.3(XRCC1):c.1605A>G (p.Pro535=)	XRCC1	Single nucleotide variant (synonymous variant)	XRCC1-related disorder	GLikely benign
Select item 3053358	NM_006297.3(XRCC1):c.925C>T (p.Pro309Ser)	XRCC1 (P309S)	Single nucleotide variant (missense variant)	XRCC1-related disorder	GLikely benign
Select item 777495	NM_006297.3(XRCC1):c.910A>G (p.Thr304Ala)	XRCC1 (T304A)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 731647	NM_006297.3(XRCC1):c.899G>A (p.Arg300Gln)	XRCC1 (R300Q)	Single nucleotide variant (missense variant)	XRCC1-related disorder +1 more	GLikely benign
Select item 3035772	NM_006297.3(XRCC1):c.667T>G (p.Ser223Ala)	XRCC1 (S223A)	Single nucleotide variant (missense variant)	XRCC1-related disorder	GLikely benign
Select item 736813	NM_006297.3(XRCC1):c.483G>A (p.Pro161=)	XRCC1	Single nucleotide variant (synonymous variant)	XRCC1-related disorder +1 more	GBenign/Likely benign
Select item 711731	NM_006297.3(XRCC1):c.215T>C (p.Val72Ala)	XRCC1 (V72A)	Single nucleotide variant (missense variant)	XRCC1-related disorder +1 more	GBenign/Likely benign
Select item 3060460	NM_006297.3(XRCC1):c.-1C>T	XRCC1	Single nucleotide variant (5 prime UTR variant)	XRCC1-related disorder	GBenign

ClinVar