List of variants in gene PALB2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 42

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.2794G>A (p.Val932Met)	rs45624036	0.00449
NM_024675.4(PALB2):c.1572A>G (p.Ser524=)	rs45472400	0.00312
NM_024675.4(PALB2):c.2590C>T (p.Pro864Ser)	rs45568339	0.00287
NM_024675.4(PALB2):c.1810C>T (p.Leu604=)	rs144015319	0.00202
NM_024675.4(PALB2):c.400G>A (p.Asp134Asn)	rs139555085	0.00160
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.1194G>A (p.Val398=)	rs61755173	0.00103
NM_024675.4(PALB2):c.909C>T (p.Leu303=)	rs145788619	0.00101
NM_024675.4(PALB2):c.2851T>C (p.Ser951Pro)	rs149522412	0.00058
NM_024675.4(PALB2):c.1470C>T (p.Pro490=)	rs45612837	0.00035
NM_024675.4(PALB2):c.2135C>T (p.Ala712Val)	rs141458731	0.00017
NM_024675.4(PALB2):c.232G>A (p.Val78Ile)	rs515726085	0.00013
NM_024675.4(PALB2):c.2379C>T (p.Gly793=)	rs377626805	0.00009
NM_024675.4(PALB2):c.344G>T (p.Gly115Val)	rs145598272	0.00009
NM_024675.4(PALB2):c.3508C>T (p.His1170Tyr)	rs200283306	0.00009
NM_024675.4(PALB2):c.2201C>A (p.Thr734Asn)	rs878855107	0.00008
NM_024675.4(PALB2):c.1935G>A (p.Glu645=)	rs141707455	0.00006
NM_024675.4(PALB2):c.768C>T (p.Ser256=)	rs45487491	0.00006
NM_024675.4(PALB2):c.13C>T (p.Pro5Ser)	rs377085677	0.00004
NM_024675.4(PALB2):c.194C>T (p.Pro65Leu)	rs62625272	0.00004
NM_024675.4(PALB2):c.2067G>A (p.Ser689=)	rs371149159	0.00004
NM_024675.4(PALB2):c.2082A>G (p.Thr694=)	rs781440401	0.00004
NM_024675.4(PALB2):c.897T>C (p.Ser299=)	rs180177095	0.00002
NM_024675.4(PALB2):c.2792T>G (p.Leu931Arg)	rs773831304	0.00001
NM_024675.4(PALB2):c.2821A>G (p.Ile941Val)	rs778602038	0.00001
NM_024675.4(PALB2):c.2922G>T (p.Lys974Asn)	rs730881892	0.00001
NM_024675.4(PALB2):c.315G>C (p.Glu105Asp)	rs515726108	0.00001
NM_024675.4(PALB2):c.3366C>T (p.Asp1122=)	rs373783514	0.00001
NM_024675.4(PALB2):c.585A>T (p.Ile195=)	rs767775306	0.00001
NM_024675.4(PALB2):c.828C>T (p.His276=)	rs911713488	0.00001
NM_024675.4(PALB2):c.834A>T (p.Leu278=)	rs199919863	0.00001
NM_024675.4(PALB2):c.1881G>T (p.Val627=)	rs139362268
NM_024675.4(PALB2):c.2031T>C (p.Val677=)	rs864622756
NM_024675.4(PALB2):c.204A>G (p.Lys68=)
NM_024675.4(PALB2):c.249C>T (p.His83=)	rs1057523390
NM_024675.4(PALB2):c.2544T>C (p.Asp848=)	rs753978124
NM_024675.4(PALB2):c.2892A>G (p.Gly964=)	rs762772267
NM_024675.4(PALB2):c.3300T>C (p.Thr1100=)
NM_024675.4(PALB2):c.3306C>T (p.Ser1102=)	rs515726112
NM_024675.4(PALB2):c.3432C>A (p.Leu1144=)	rs748363227
NM_024675.4(PALB2):c.85A>G (p.Ser29Gly)	rs776110440

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