List of variants in gene combination RAD51D, RAD51L3-RFFL reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.481-7G>A	rs145832514	0.00171
NM_002878.4(RAD51D):c.568G>A (p.Ala190Thr)	rs80116829	0.00167
NM_002878.4(RAD51D):c.263+1588A>G	rs180869630	0.00123
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser)	rs140825795	0.00037
NM_002878.4(RAD51D):c.216C>T (p.Tyr72=)	rs148690585	0.00028
NM_002878.4(RAD51D):c.904-3C>T	rs45478491	0.00018
NM_002878.4(RAD51D):c.263+1474C>T	rs201720876	0.00016
NM_002878.4(RAD51D):c.145-4G>A	rs201361465	0.00006
NM_002878.4(RAD51D):c.263+1641C>T	rs142387263	0.00006
NM_002878.4(RAD51D):c.715C>T (p.Arg239Trp)	rs770250516	0.00006
NM_002878.4(RAD51D):c.493C>T (p.Arg165Trp)	rs544654228	0.00004
NM_002878.4(RAD51D):c.694C>T (p.Arg232Ter)	rs587780104	0.00004
NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter)	rs387906843	0.00003
NM_002878.4(RAD51D):c.451C>T (p.Gln151Ter)	rs587781756	0.00002
NM_002878.4(RAD51D):c.620C>T (p.Ser207Leu)	rs370228071	0.00002
NM_002878.4(RAD51D):c.621G>T (p.Ser207=)	rs749859221	0.00001
NM_002878.4(RAD51D):c.900A>G (p.Arg300=)	rs370634278	0.00001
NM_002878.4(RAD51D):c.163C>T (p.Arg55Trp)	rs775268017
NM_002878.4(RAD51D):c.231C>G (p.Thr77=)	rs376670250
NM_002878.4(RAD51D):c.263+1571T>C
NM_002878.4(RAD51D):c.263+1631C>T
NM_002878.4(RAD51D):c.270_271dup (p.Lys91fs)	rs753862052
NM_002878.4(RAD51D):c.294T>C (p.Tyr98=)
NM_002878.4(RAD51D):c.357_360del (p.Cys119fs)	rs876658297
NM_002878.4(RAD51D):c.370G>A (p.Val124Met)	rs776581316
NM_002878.4(RAD51D):c.412A>C (p.Asn138His)	rs141690729
NM_002878.4(RAD51D):c.426A>G (p.Thr142=)	rs1597862600
NM_002878.4(RAD51D):c.708C>T (p.Thr236=)
NM_002878.4(RAD51D):c.71G>A (p.Arg24Lys)	rs947444435

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