List of variants in gene PALB2 reported as likely benign for exocrine pancreatic carcinoma

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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: 38

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HGVS	dbSNP	gnomAD frequency
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.2993G>A (p.Gly998Glu)	rs45551636	0.01717
NM_024675.4(PALB2):c.2590C>T (p.Pro864Ser)	rs45568339	0.00287
NM_024675.4(PALB2):c.1606C>T (p.Leu536=)	rs151162255	0.00193
NM_024675.4(PALB2):c.2996+17T>C	rs180177128	0.00060
NM_024675.4(PALB2):c.1470C>T (p.Pro490=)	rs45612837	0.00035
NM_024675.4(PALB2):c.1281T>C (p.Ala427=)	rs138697796	0.00021
NM_024675.4(PALB2):c.2135C>T (p.Ala712Val)	rs141458731	0.00017
NM_024675.4(PALB2):c.1794G>A (p.Leu598=)	rs182494675	0.00015
NM_024675.4(PALB2):c.1455T>G (p.Thr485=)	rs566105533	0.00011
NM_024675.4(PALB2):c.2032C>T (p.Leu678=)	rs376189676	0.00007
NM_024675.4(PALB2):c.1935G>A (p.Glu645=)	rs141707455	0.00006
NM_024675.4(PALB2):c.3297G>A (p.Thr1099=)	rs45565738	0.00006
NM_024675.4(PALB2):c.765T>C (p.Asp255=)	rs45465299	0.00006
NM_024675.4(PALB2):c.2834+13C>A	rs551516577	0.00004
NM_024675.4(PALB2):c.3252G>A (p.Ser1084=)	rs141570833	0.00004
NM_024675.4(PALB2):c.900A>G (p.Thr300=)	rs771660444	0.00004
NM_024675.4(PALB2):c.1272C>T (p.Ala424=)	rs754720030	0.00003
NM_024675.4(PALB2):c.3432C>T (p.Leu1144=)	rs748363227	0.00002
NM_024675.4(PALB2):c.1164T>C (p.Pro388=)	rs1205215998	0.00001
NM_024675.4(PALB2):c.195G>A (p.Pro65=)	rs751176316	0.00001
NM_024675.4(PALB2):c.2587-12C>T	rs1266683395	0.00001
NM_024675.4(PALB2):c.2784G>A (p.Val928=)	rs763411245	0.00001
NM_024675.4(PALB2):c.2881C>T (p.Leu961=)	rs61755166	0.00001
NM_024675.4(PALB2):c.2985A>T (p.Ala995=)	rs786202892	0.00001
NM_024675.4(PALB2):c.3202-9C>T	rs757444247	0.00001
NM_024675.4(PALB2):c.3350+16T>G	rs515726115	0.00001
NM_024675.4(PALB2):c.735G>A (p.Ala245=)	rs371612049	0.00001
NM_024675.4(PALB2):c.108+7_108+8delinsAT	rs2142459585
NM_024675.4(PALB2):c.1482T>C (p.Thr494=)	rs2142414557
NM_024675.4(PALB2):c.168T>C (p.Asp56=)	rs1203135643
NM_024675.4(PALB2):c.1881G>T (p.Val627=)	rs139362268
NM_024675.4(PALB2):c.18G>A (p.Gly6=)	rs587782462
NM_024675.4(PALB2):c.212-24TA[4]	rs751741705
NM_024675.4(PALB2):c.2424A>C (p.Gly808=)	rs1060504714
NM_024675.4(PALB2):c.2834+13C>G	rs551516577
NM_024675.4(PALB2):c.3204G>T (p.Gly1068=)	rs786203475

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