List of variants in gene PALB2 reported as uncertain significance 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: 41

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HGVS	dbSNP	gnomAD frequency
NM_024675.4(PALB2):c.1564C>T (p.Pro522Ser)	rs373876101	0.00016
NM_024675.4(PALB2):c.3054G>C (p.Glu1018Asp)	rs183489969	0.00016
NM_024675.4(PALB2):c.11C>T (p.Pro4Leu)	rs45619737	0.00010
NM_024675.4(PALB2):c.2379C>T (p.Gly793=)	rs377626805	0.00009
NM_024675.4(PALB2):c.3251C>T (p.Ser1084Leu)	rs62625271	0.00009
NM_024675.4(PALB2):c.2200A>T (p.Thr734Ser)	rs45543843	0.00007
NM_024675.4(PALB2):c.1273G>A (p.Val425Met)	rs576081828	0.00006
NM_024675.4(PALB2):c.2289G>C (p.Leu763Phe)	rs373478248	0.00004
NM_024675.4(PALB2):c.1766C>T (p.Thr589Met)	rs773340677	0.00003
NM_024675.4(PALB2):c.2743G>A (p.Ala915Thr)	rs374736398	0.00003
NM_024675.4(PALB2):c.2748+15C>T	rs749756493	0.00003
NM_024675.4(PALB2):c.3146T>C (p.Met1049Thr)	rs138273800	0.00003
NM_024675.4(PALB2):c.94C>G (p.Leu32Val)	rs151316635	0.00003
NM_024675.4(PALB2):c.950C>T (p.Thr317Ile)	rs45548638	0.00003
NM_024675.4(PALB2):c.149A>C (p.Lys50Thr)	rs763598472	0.00002
NM_024675.4(PALB2):c.2417C>T (p.Pro806Leu)	rs45464991	0.00002
NM_024675.4(PALB2):c.2612A>G (p.Asp871Gly)	rs515726090	0.00002
NM_024675.4(PALB2):c.995T>A (p.Leu332His)	rs377149139	0.00002
NM_024675.4(PALB2):c.1446C>G (p.Leu482=)	rs368759893	0.00001
NM_024675.4(PALB2):c.1597A>G (p.Thr533Ala)	rs1393117824	0.00001
NM_024675.4(PALB2):c.2342G>A (p.Ser781Asn)	rs761298847	0.00001
NM_024675.4(PALB2):c.2344C>T (p.Pro782Ser)	rs786203296	0.00001
NM_024675.4(PALB2):c.2435C>T (p.Pro812Leu)	rs774502617	0.00001
NM_024675.4(PALB2):c.2792T>G (p.Leu931Arg)	rs773831304	0.00001
NM_024675.4(PALB2):c.2922G>T (p.Lys974Asn)	rs730881892	0.00001
NM_024675.4(PALB2):c.3278T>C (p.Ile1093Thr)	rs45616636	0.00001
NM_024675.4(PALB2):c.660T>C (p.Ser220=)	rs571762192	0.00001
NM_024675.4(PALB2):c.824C>T (p.Thr275Ile)	rs786202499	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.1837C>G (p.Gln613Glu)	rs1966865214
NM_024675.4(PALB2):c.1843C>T (p.Pro615Ser)	rs1019525144
NM_024675.4(PALB2):c.2188A>G (p.Ile730Val)	rs1060502735
NM_024675.4(PALB2):c.2615T>C (p.Val872Ala)	rs730881877
NM_024675.4(PALB2):c.2852C>T (p.Ser951Phe)	rs587782889
NM_024675.4(PALB2):c.2996+3A>G	rs876659931
NM_024675.4(PALB2):c.3031G>A (p.Glu1011Lys)	rs1302512878
NM_024675.4(PALB2):c.3095T>G (p.Met1032Arg)	rs745562326
NM_024675.4(PALB2):c.3418T>G (p.Trp1140Gly)	rs62625283
NM_024675.4(PALB2):c.457A>C (p.Arg153=)	rs1375458252
NM_024675.4(PALB2):c.833_834delinsAT (p.Leu278His)	rs587778582

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