List of variants in gene PALB2 reported as benign for Hereditary cancer-predisposing syndrome

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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: 42

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.1676A>G (p.Gln559Arg)	rs152451	0.12980
NM_024675.4(PALB2):c.-47G>A	rs8053188	0.04991
NM_024675.4(PALB2):c.3300T>G (p.Thr1100=)	rs45516100	0.02529
NM_024675.4(PALB2):c.2014G>C (p.Glu672Gln)	rs45532440	0.02171
NM_024675.4(PALB2):c.212-58A>C	rs80291632	0.02171
NM_024675.4(PALB2):c.629C>T (p.Pro210Leu)	rs57605939	0.02101
NM_024675.4(PALB2):c.1684+29A>G	rs74320059	0.01884
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.925A>G (p.Ile309Val)	rs3809683	0.00919
NM_024675.4(PALB2):c.53A>G (p.Lys18Arg)	rs138789658	0.00530
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.1419A>C (p.Pro473=)	rs62625275	0.00309
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.721A>G (p.Asn241Asp)	rs113217267	0.00202
NM_024675.4(PALB2):c.1606C>T (p.Leu536=)	rs151162255	0.00193
NM_024675.4(PALB2):c.2256A>G (p.Gly752=)	rs147120218	0.00193
NM_024675.4(PALB2):c.400G>A (p.Asp134Asn)	rs139555085	0.00160
NM_024675.4(PALB2):c.2742C>T (p.Phe914=)	rs115759702	0.00143
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.2851T>C (p.Ser951Pro)	rs149522412	0.00058
NM_024675.4(PALB2):c.1000T>G (p.Tyr334Asp)	rs202241382	0.00026
NM_024675.4(PALB2):c.298C>T (p.Leu100Phe)	rs61756147	0.00021
NM_024675.4(PALB2):c.1492G>T (p.Asp498Tyr)	rs75023630	0.00020
NM_024675.4(PALB2):c.2135C>T (p.Ala712Val)	rs141458731	0.00017
NM_024675.4(PALB2):c.3054G>C (p.Glu1018Asp)	rs183489969	0.00016
NM_024675.4(PALB2):c.2027T>C (p.Ile676Thr)	rs200875161	0.00011
NM_024675.4(PALB2):c.1623G>A (p.Arg541=)	rs745665968	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.765T>C (p.Asp255=)	rs45465299	0.00006
NM_024675.4(PALB2):c.950C>T (p.Thr317Ile)	rs45548638	0.00003
NM_024675.4(PALB2):c.2417C>T (p.Pro806Leu)	rs45464991	0.00002
NM_024675.4(PALB2):c.2258G>A (p.Arg753Gln)	rs587778586	0.00001
NM_024675.4(PALB2):c.734C>T (p.Ala245Val)	rs571063157	0.00001
NM_024675.4(PALB2):c.899C>T (p.Thr300Ile)	rs528541334	0.00001
NM_024675.4(PALB2):c.928A>G (p.Ser310Gly)	rs45561331	0.00001
NM_024675.4(PALB2):c.2607C>T (p.Ser869=)	rs45542234

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