List of variants in gene PALB2 reported as likely benign for Malignant tumor of breast

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.2993G>A (p.Gly998Glu)	rs45551636	0.01717
NM_024675.4(PALB2):c.1010T>C (p.Leu337Ser)	rs45494092	0.01508
NM_024675.4(PALB2):c.721A>G (p.Asn241Asp)	rs113217267	0.00202
NM_024675.4(PALB2):c.1606C>T (p.Leu536=)	rs151162255	0.00193
NM_024675.4(PALB2):c.2816T>G (p.Leu939Trp)	rs45478192	0.00121
NM_024675.4(PALB2):c.3495G>A (p.Ser1165=)	rs45439097	0.00121
NM_024675.4(PALB2):c.909C>T (p.Leu303=)	rs145788619	0.00101
NM_024675.4(PALB2):c.1492G>T (p.Asp498Tyr)	rs75023630	0.00020
NM_024675.4(PALB2):c.232G>A (p.Val78Ile)	rs515726085	0.00013
NM_024675.4(PALB2):c.344G>T (p.Gly115Val)	rs145598272	0.00009
NM_024675.4(PALB2):c.2509G>A (p.Glu837Lys)	rs587778587	0.00008
NM_024675.4(PALB2):c.768C>T (p.Ser256=)	rs45487491	0.00006
NM_024675.4(PALB2):c.2442G>A (p.Glu814=)	rs140776736	0.00005
NM_024675.4(PALB2):c.21G>A (p.Lys7=)	rs1424944402	0.00001
NM_024675.4(PALB2):c.2505C>T (p.Ser835=)	rs756502783	0.00001
NM_024675.4(PALB2):c.3024C>T (p.Pro1008=)	rs180177130	0.00001
NM_024675.4(PALB2):c.828C>T (p.His276=)	rs911713488	0.00001
NM_024675.4(PALB2):c.1095G>A (p.Arg365=)	rs515726062
NM_024675.4(PALB2):c.1242A>C (p.Arg414=)	rs875989795
NM_024675.4(PALB2):c.1278G>A (p.Glu426=)	rs1555461362
NM_024675.4(PALB2):c.2996+9del	rs769414858
NM_024675.4(PALB2):c.426G>A (p.Lys142=)	rs1967047677

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