ClinVar Miner

List of variants in gene PALB2 reported as uncertain significance for Hereditary breast ovarian cancer syndrome

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_024675.4(PALB2):c.23C>T (p.Pro8Leu) rs150390726 0.00051
NM_024675.4(PALB2):c.1492G>T (p.Asp498Tyr) rs75023630 0.00020
NM_024675.4(PALB2):c.3054G>C (p.Glu1018Asp) rs183489969 0.00016
NM_024675.4(PALB2):c.2586+30G>A rs769118926 0.00009
NM_024675.4(PALB2):c.2509G>A (p.Glu837Lys) rs587778587 0.00008
NM_024675.4(PALB2):c.1379A>G (p.Gln460Arg) rs749494645 0.00002
NM_024675.4(PALB2):c.1955G>A (p.Ser652Asn) rs587781818 0.00002
NM_024675.4(PALB2):c.3331C>G (p.Pro1111Ala) rs864622193 0.00001
NM_024675.4(PALB2):c.3379T>C (p.Cys1127Arg) rs767830005 0.00001
NM_024675.4(PALB2):c.661G>A (p.Val221Ile) rs1060502773 0.00001
NG_007406.1:g.?_?ins(23632682_23625413)_(23625324_23619334)
NM_024675.4(PALB2):c.1684+18TGA[6] rs368593832
NM_024675.4(PALB2):c.25C>T (p.Leu9Phe) rs1060502744
NM_024675.4(PALB2):c.2891_2905del (p.Gly964_Ala968del) rs1966802547
NM_024675.4(PALB2):c.2996+4A>G
NM_024675.4(PALB2):c.3089C>T (p.Thr1030Ile) rs876660109
NM_024675.4(PALB2):c.3296C>T (p.Thr1099Met) rs142132127
NM_024675.4(PALB2):c.3307G>A (p.Val1103Met) rs201657283
NM_024675.4(PALB2):c.3350G>A (p.Arg1117Lys) rs876659859
NM_024675.4(PALB2):c.474G>C (p.Gln158His) rs878855119

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