List of variants in gene combination RAD51D, RAD51L3-RFFL reported as uncertain significance for Hereditary breast ovarian cancer syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 50

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.146C>T (p.Ala49Val)	rs140317560	0.00116
NM_002878.4(RAD51D):c.932T>A (p.Ile311Asn)	rs145309168	0.00041
NM_002878.4(RAD51D):c.904-11T>A	rs374449943	0.00038
NM_002878.4(RAD51D):c.196G>A (p.Val66Met)	rs56026142	0.00009
NM_002878.4(RAD51D):c.864C>T (p.Gly288=)	rs138557828	0.00009
NM_002878.4(RAD51D):c.973G>A (p.Gly325Ser)	rs587780106	0.00008
NM_002878.4(RAD51D):c.629C>T (p.Ala210Val)	rs376855484	0.00006
NM_002878.4(RAD51D):c.29C>T (p.Pro10Leu)	rs759505297	0.00005
NM_002878.4(RAD51D):c.185C>T (p.Ser62Leu)	rs374357106	0.00004
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys)	rs587781813	0.00004
NM_002878.4(RAD51D):c.202G>A (p.Gly68Ser)	rs775045445	0.00003
NM_002878.4(RAD51D):c.208G>A (p.Asp70Asn)	rs142189122	0.00003
NM_002878.4(RAD51D):c.164G>A (p.Arg55Gln)	rs151198586	0.00002
NM_002878.4(RAD51D):c.899G>A (p.Arg300Gln)	rs761290755	0.00002
NM_002878.4(RAD51D):c.56T>C (p.Leu19Pro)	rs1044486334	0.00001
NM_002878.4(RAD51D):c.607G>A (p.Val203Met)	rs730881947	0.00001
NM_002878.4(RAD51D):c.619T>C (p.Ser207Pro)	rs372365287	0.00001
NM_002878.4(RAD51D):c.716G>A (p.Arg239Gln)	rs780921112	0.00001
NM_002878.4(RAD51D):c.80C>A (p.Thr27Lys)	rs139642328	0.00001
NM_002878.4(RAD51D):c.823C>T (p.Arg275Trp)	rs752780416	0.00001
NM_002878.4(RAD51D):c.871C>T (p.Arg291Cys)	rs372038369	0.00001
NM_002878.4(RAD51D):c.955C>T (p.Gln319Ter)	rs794726988	0.00001
NM_002878.4(RAD51D):c.109G>C (p.Glu37Gln)	rs876659848
NM_002878.4(RAD51D):c.141C>T (p.Tyr47=)	rs771077929
NM_002878.4(RAD51D):c.145-9C>G
NM_002878.4(RAD51D):c.192C>T (p.Phe64=)	rs1567735397
NM_002878.4(RAD51D):c.1A>G (p.Met1Val)	rs561425038
NM_002878.4(RAD51D):c.232T>G (p.Ser78Ala)	rs1567735315
NM_002878.4(RAD51D):c.263+1450T>A	rs1567734484
NM_002878.4(RAD51D):c.263+1551G>T	rs780006577
NM_002878.4(RAD51D):c.263+1642G>T	rs773367679
NM_002878.4(RAD51D):c.339A>C (p.Lys113Asn)	rs786202507
NM_002878.4(RAD51D):c.345G>A (p.Gln115=)	rs1555568469
NM_002878.4(RAD51D):c.361G>A (p.Ala121Thr)	rs1555568366
NM_002878.4(RAD51D):c.401A>G (p.Tyr134Cys)	rs1567728366
NM_002878.4(RAD51D):c.422T>C (p.Leu141Pro)	rs780938875
NM_002878.4(RAD51D):c.481G>T (p.Ala161Ser)	rs1567727951
NM_002878.4(RAD51D):c.493C>G (p.Arg165Gly)	rs544654228
NM_002878.4(RAD51D):c.573G>A (p.Gln191=)	rs1597861626
NM_002878.4(RAD51D):c.575A>G (p.Gln192Arg)	rs876660090
NM_002878.4(RAD51D):c.576G>A (p.Gln192=)	rs2091602856
NM_002878.4(RAD51D):c.754A>C (p.Thr252Pro)	rs1173524549
NM_002878.4(RAD51D):c.785C>T (p.Pro262Leu)	rs730881950
NM_002878.4(RAD51D):c.806G>A (p.Ser269Asn)	rs876658762
NM_002878.4(RAD51D):c.80C>T (p.Thr27Ile)	rs139642328
NM_002878.4(RAD51D):c.83-3C>G	rs1555570424
NM_002878.4(RAD51D):c.835G>A (p.Asp279Asn)	rs765271127
NM_002878.4(RAD51D):c.86T>C (p.Val29Ala)	rs1567735899
NM_002878.4(RAD51D):c.875T>C (p.Met292Thr)
NM_002878.4(RAD51D):c.904-2A>T	rs1403784434

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