List of variants in gene PALLD reported as likely benign for adenocarcinoma

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: 90

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001166108.2(PALLD):c.1965-12636G>A	rs543821321	0.00160
NM_001166108.2(PALLD):c.1965-12908G>A	rs758706279	0.00107
NM_001166108.2(PALLD):c.1965-12840C>G	rs587780757	0.00020
NM_001166108.2(PALLD):c.1965-12857G>A	rs952110792	0.00008
NM_001166108.2(PALLD):c.1965-12569G>A	rs568490721	0.00007
NM_001166108.2(PALLD):c.1965-12817C>T	rs1211489449	0.00007
NM_001166108.2(PALLD):c.1965-13025C>T	rs952079408	0.00005
NM_001166108.2(PALLD):c.1965-12574C>T	rs763225090	0.00004
NM_001166108.2(PALLD):c.1965-12896C>T	rs1319983866	0.00004
NM_001166108.2(PALLD):c.1965-12898C>A	rs1025237623	0.00004
NM_001166108.2(PALLD):c.1965-12635C>T	rs1385998898	0.00003
NM_001166108.2(PALLD):c.1965-12737C>T	rs1060504775	0.00003
NM_001166108.2(PALLD):c.1965-12803G>A	rs1477864263	0.00003
NM_001166108.2(PALLD):c.1965-12944G>C	rs1231114395	0.00003
NM_001166108.2(PALLD):c.1965-12950C>T	rs1346040206	0.00003
NM_001166108.2(PALLD):c.1965-13001C>G	rs1239099971	0.00003
NM_001166108.2(PALLD):c.1965-12514G>A	rs1355423115	0.00002
NM_001166108.2(PALLD):c.1965-12566C>T	rs864622158	0.00002
NM_001166108.2(PALLD):c.1965-12587C>T	rs1460784357	0.00002
NM_001166108.2(PALLD):c.1965-12592C>T	rs1400689367	0.00002
NM_001166108.2(PALLD):c.1965-12800C>T	rs863224383	0.00002
NM_001166108.2(PALLD):c.1965-12875G>A	rs587780755	0.00002
NM_001166108.2(PALLD):c.1965-12962C>T	rs987749164	0.00002
NM_001166108.2(PALLD):c.1965-12519C>G	rs1358006173	0.00001
NM_001166108.2(PALLD):c.1965-12556C>T	rs878854265	0.00001
NM_001166108.2(PALLD):c.1965-12575G>A	rs554297134	0.00001
NM_001166108.2(PALLD):c.1965-12617G>A	rs1046350904	0.00001
NM_001166108.2(PALLD):c.1965-12686G>A	rs1275232115	0.00001
NM_001166108.2(PALLD):c.1965-12703C>T	rs1232895995	0.00001
NM_001166108.2(PALLD):c.1965-12718C>T	rs570874237	0.00001
NM_001166108.2(PALLD):c.1965-12735C>G	rs1434151476	0.00001
NM_001166108.2(PALLD):c.1965-12866C>T	rs996343137	0.00001
NM_001166108.2(PALLD):c.1965-12872C>T	rs1752030193	0.00001
NM_001166108.2(PALLD):c.1965-12878G>A	rs1752028956	0.00001
NM_001166108.2(PALLD):c.1965-12890G>A	rs1252109828	0.00001
NM_001166108.2(PALLD):c.1965-12968G>A	rs1442067136	0.00001
NM_001166108.2(PALLD):c.1965-12971C>T	rs752730979	0.00001
NM_001166108.2(PALLD):c.1965-8T>C	rs1374341509	0.00001
NM_001166108.2(PALLD):c.1965-9dup	rs769161509	0.00001
NM_001166108.2(PALLD):c.2007C>T (p.Ser669=)	rs561075148	0.00001
NM_001166108.2(PALLD):c.2100+12T>G	rs1178801747	0.00001
NM_001166108.2(PALLD):c.1965-12515C>G
NM_001166108.2(PALLD):c.1965-12515C>T
NM_001166108.2(PALLD):c.1965-12536C>T	rs2151120978
NM_001166108.2(PALLD):c.1965-12554G>C
NM_001166108.2(PALLD):c.1965-12563C>T	rs2151120642
NM_001166108.2(PALLD):c.1965-12572G>A
NM_001166108.2(PALLD):c.1965-12575G>C	rs554297134
NM_001166108.2(PALLD):c.1965-12590G>A
NM_001166108.2(PALLD):c.1965-12599C>T	rs900642927
NM_001166108.2(PALLD):c.1965-12602C>T	rs1002022068
NM_001166108.2(PALLD):c.1965-12605C>T	rs1553965526
NM_001166108.2(PALLD):c.1965-12641C>T	rs1553965480
NM_001166108.2(PALLD):c.1965-12656C>T
NM_001166108.2(PALLD):c.1965-12665G>A	rs535155432
NM_001166108.2(PALLD):c.1965-12671G>C
NM_001166108.2(PALLD):c.1965-12677G>A
NM_001166108.2(PALLD):c.1965-12683G>A	rs864622321
NM_001166108.2(PALLD):c.1965-12692A>C	rs864622591
NM_001166108.2(PALLD):c.1965-12704A>G	rs863224386
NM_001166108.2(PALLD):c.1965-12725C>T
NM_001166108.2(PALLD):c.1965-12761C>A
NM_001166108.2(PALLD):c.1965-12761C>T
NM_001166108.2(PALLD):c.1965-12764G>T
NM_001166108.2(PALLD):c.1965-12773G>C	rs1240958245
NM_001166108.2(PALLD):c.1965-12782C>A	rs2151117841
NM_001166108.2(PALLD):c.1965-12809C>T
NM_001166108.2(PALLD):c.1965-12812C>T	rs532961259
NM_001166108.2(PALLD):c.1965-12821G>A
NM_001166108.2(PALLD):c.1965-12830G>T	rs587780758
NM_001166108.2(PALLD):c.1965-12836C>G	rs1752038882
NM_001166108.2(PALLD):c.1965-12854G>A
NM_001166108.2(PALLD):c.1965-12860G>A
NM_001166108.2(PALLD):c.1965-12911G>T
NM_001166108.2(PALLD):c.1965-12923G>A	rs2151116162
NM_001166108.2(PALLD):c.1965-12926G>C
NM_001166108.2(PALLD):c.1965-12935C>A
NM_001166108.2(PALLD):c.1965-12941G>A	rs864622590
NM_001166108.2(PALLD):c.1965-12944G>A	rs1231114395
NM_001166108.2(PALLD):c.1965-12947C>G	rs1279362848
NM_001166108.2(PALLD):c.1965-12947C>T
NM_001166108.2(PALLD):c.1965-12974C>T	rs1314232427
NM_001166108.2(PALLD):c.1965-12986C>T	rs1405467936
NM_001166108.2(PALLD):c.1965-13004C>T
NM_001166108.2(PALLD):c.1965-13019G>A
NM_001166108.2(PALLD):c.1965-13022G>A	rs1305250587
NM_001166108.2(PALLD):c.1965-17G>C
NM_001166108.2(PALLD):c.1965-19T>C
NM_001166108.2(PALLD):c.1986T>C (p.Ser662=)	rs774706421
NM_001166108.2(PALLD):c.2085G>T (p.Leu695=)	rs2151193953

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.