ClinVar Miner

List of variants in gene PALLD reported as uncertain significance for Pancreatic cancer, susceptibility to, 1

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001166108.2(PALLD):c.1394G>A (p.Arg465His) rs115372194 0.00111
NM_001166108.2(PALLD):c.-83+9G>A rs150719521 0.00037
NM_001166108.2(PALLD):c.-143A>G rs571957605 0.00023
NM_001166108.2(PALLD):c.1965-12840C>G rs587780757 0.00019
NM_001166108.2(PALLD):c.-135A>G rs540285834 0.00015
NM_001166108.2(PALLD):c.349G>T (p.Val117Phe) rs375246198 0.00015
NM_001166108.2(PALLD):c.-115C>G rs189011214 0.00012
NM_001166108.2(PALLD):c.264A>C (p.Glu88Asp) rs202095635 0.00007
NM_001166108.2(PALLD):c.428G>A (p.Arg143His) rs149345491 0.00007
NM_001166108.2(PALLD):c.2084T>G (p.Leu695Arg) rs139375029 0.00006
NM_001166108.2(PALLD):c.556G>A (p.Ala186Thr) rs139434937 0.00005
NM_001166108.2(PALLD):c.1266C>G (p.His422Gln) rs147159943 0.00004
NM_001166108.2(PALLD):c.1433G>A (p.Gly478Glu) rs201816881 0.00004
NM_001166108.2(PALLD):c.215C>T (p.Pro72Leu) rs756698993 0.00003
NM_001166108.2(PALLD):c.1129A>G (p.Lys377Glu) rs368684220 0.00002
NM_001166108.2(PALLD):c.1412A>T (p.Gln471Leu) rs923352111 0.00002
NM_001166108.2(PALLD):c.860G>A (p.Arg287Gln) rs141283998 0.00002
NM_001166108.2(PALLD):c.-172C>A rs777479051 0.00001
NM_001166108.2(PALLD):c.-178G>A rs886059207 0.00001
NM_001166108.2(PALLD):c.107A>G (p.Gln36Arg) rs889514388 0.00001
NM_001166108.2(PALLD):c.1135A>G (p.Arg379Gly) rs1348758631 0.00001
NM_001166108.2(PALLD):c.1219A>T (p.Thr407Ser) rs775730191 0.00001
NM_001166108.2(PALLD):c.1256A>C (p.Gln419Pro) rs761386762 0.00001
NM_001166108.2(PALLD):c.1260+8T>C rs887513464 0.00001
NM_001166108.2(PALLD):c.1268G>T (p.Ser423Ile) rs1781943093 0.00001
NM_001166108.2(PALLD):c.1571G>T (p.Arg524Ile) rs776908136 0.00001
NM_001166108.2(PALLD):c.1681C>A (p.His561Asn) rs763814940 0.00001
NM_001166108.2(PALLD):c.1811A>G (p.Asn604Ser) rs948639021 0.00001
NM_001166108.2(PALLD):c.2057G>A (p.Arg686Gln) rs1031710807 0.00001
NM_001166108.2(PALLD):c.2099C>T (p.Pro700Leu) rs1255873290 0.00001
NM_001166108.2(PALLD):c.222C>T (p.Ser74=) rs201038000 0.00001
NM_001166108.2(PALLD):c.593C>T (p.Ser198Leu) rs770328647 0.00001
NM_001166108.2(PALLD):c.836G>C (p.Ser279Thr) rs886059209 0.00001
NM_001166108.2(PALLD):c.1155-16C>A
NM_001166108.2(PALLD):c.1502-9C>T
NM_001166108.2(PALLD):c.1616C>T (p.Thr539Ile) rs780510622
NM_001166108.2(PALLD):c.164C>A (p.Thr55Lys) rs1554032915
NM_001166108.2(PALLD):c.1850G>A (p.Arg617His)
NM_001166108.2(PALLD):c.1926C>G (p.Pro642=) rs886059210
NM_001166108.2(PALLD):c.1942C>T (p.Pro648Ser) rs1784871346
NM_001166108.2(PALLD):c.1957C>A (p.Pro653Thr) rs1784873065
NM_001166108.2(PALLD):c.2027C>A (p.Thr676Lys) rs368056641
NM_001166108.2(PALLD):c.2063T>G (p.Leu688Arg) rs2533587935
NM_001166108.2(PALLD):c.236C>G (p.Pro79Arg)
NM_001166108.2(PALLD):c.301C>T (p.Pro101Ser)
NM_001166108.2(PALLD):c.34G>A (p.Asp12Asn)
NM_001166108.2(PALLD):c.569A>G (p.Asn190Ser) rs2531433996
NM_001166108.2(PALLD):c.574A>G (p.Ser192Gly) rs1762575507
NM_001166108.2(PALLD):c.622A>G (p.Lys208Glu) rs1762580055
NM_001166108.2(PALLD):c.639C>A (p.Ala213=) rs1762581096
NM_001166108.2(PALLD):c.721C>T (p.His241Tyr) rs1490249027
NM_001166108.2(PALLD):c.815G>A (p.Arg272Gln) rs140415820
NM_001166108.2(PALLD):c.855G>T (p.Gly285=)
NM_001166108.2(PALLD):c.876_877insCTGG (p.Arg293fs)
NM_001166108.2(PALLD):c.908+3A>G rs1762604026
NM_001166108.2(PALLD):c.946G>T (p.Asp316Tyr) rs1477916241

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.