ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 29
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HGVS dbSNP
NM_002878.3(RAD51D):c.*106G>A rs45494001
NM_002878.3(RAD51D):c.*1082C>T rs774128458
NM_002878.3(RAD51D):c.*130A>C rs28363292
NM_002878.3(RAD51D):c.*154T>A rs886052816
NM_002878.3(RAD51D):c.*254T>G rs778094856
NM_002878.3(RAD51D):c.*366C>T rs12947947
NM_002878.3(RAD51D):c.*367G>A rs28363293
NM_002878.3(RAD51D):c.*373G>A rs28363294
NM_002878.3(RAD51D):c.*433_*434delCT rs757426326
NM_002878.3(RAD51D):c.*555A>G rs142021403
NM_002878.3(RAD51D):c.*710G>A rs28363296
NM_002878.3(RAD51D):c.*715G>A rs188627847
NM_002878.3(RAD51D):c.*875_*878delCAGA rs754041004
NM_002878.3(RAD51D):c.-139C>T rs886052820
NM_002878.3(RAD51D):c.-164G>A rs549819451
NM_002878.3(RAD51D):c.-238A>T rs188262287
NM_002878.3(RAD51D):c.-239C>T rs550346401
NM_002878.3(RAD51D):c.-38G>T rs114252524
NM_002878.3(RAD51D):c.-73G>A rs886052819
NM_002878.3(RAD51D):c.196G>A (p.Val66Met) rs56026142
NM_002878.3(RAD51D):c.208G>A (p.Asp70Asn) rs142189122
NM_002878.3(RAD51D):c.234C>T (p.Ser78=) rs9901455
NM_002878.3(RAD51D):c.481-8C>T rs762247126
NM_002878.3(RAD51D):c.494G>A (p.Arg165Gln) rs4796033
NM_002878.3(RAD51D):c.698A>G (p.Glu233Gly) rs28363284
NM_002878.3(RAD51D):c.873C>T (p.Arg291=) rs140848654
NM_002878.3(RAD51D):c.929A>C (p.Asp310Ala) rs886052818
NM_002878.3(RAD51D):c.933T>G (p.Ile311Met) rs886052817
NM_002878.3(RAD51D):c.983C>T (p.Thr328Ile) rs138969595

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