ClinVar Miner

List of variants reported as likely pathogenic by Cancer Genetics Laboratory,Peter MacCallum Cancer Centre

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Total variants: 19
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HGVS dbSNP
NM_024675.3(PALB2):c.168_171TTGT[1] (p.Gln60fs) rs180177143
NM_024675.3(PALB2):c.1947_1966dup (p.Pro656fs) rs1555460564
NM_024675.3(PALB2):c.1947dup (p.Glu650fs) rs515726075
NM_024675.3(PALB2):c.196C>T (p.Gln66Ter) rs180177083
NM_024675.3(PALB2):c.2386G>T (p.Gly796Ter) rs180177112
NM_024675.3(PALB2):c.2391del (p.Gln797fs) rs1555460360
NM_024675.3(PALB2):c.2959_2966dup (p.Glu990fs) rs875989792
NM_024675.3(PALB2):c.2982dup (p.Ala995fs) rs180177127
NM_024675.3(PALB2):c.3113G>A (p.Trp1038Ter) rs180177132
NM_024675.3(PALB2):c.3116del (p.Asn1039fs) rs180177133
NM_024675.3(PALB2):c.3256C>T (p.Arg1086Ter) rs587776527
NM_024675.3(PALB2):c.3362del (p.Gly1121fs) rs515726117
NM_024675.3(PALB2):c.3505_3506TC[1] (p.His1170fs) rs587776428
NM_024675.3(PALB2):c.3549C>G (p.Tyr1183Ter) rs118203998
NM_024675.3(PALB2):c.522_523del (p.Arg175fs) rs875989789
NM_024675.3(PALB2):c.577dup (p.Thr193fs) rs875989790
NM_024675.3(PALB2):c.693dup (p.Gly232fs) rs875989791
NM_024675.3(PALB2):c.758dup (p.Ser254fs) rs515726126
NM_024675.3(PALB2):c.860dup (p.Ser288fs) rs864622301

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