ClinVar Miner

List of variants in gene CBR4, PALLD studied for Pancreatic cancer, susceptibility to, 1

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 57
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001166108.2(PALLD):c.*2058C>G rs1071738 0.51499
NM_001166108.2(PALLD):c.*317A>T rs542531106 0.23477
NM_001166108.2(PALLD):c.2679A>G (p.Arg893=) rs1059444 0.12743
NM_001166108.2(PALLD):c.*1906G>A rs1136603 0.12735
NM_001166108.2(PALLD):c.3359-4G>A rs112116419 0.01744
NM_001166108.2(PALLD):c.*992A>G rs28718025 0.01242
NM_001166108.2(PALLD):c.*1164T>G rs114351964 0.01238
NM_001166108.2(PALLD):c.3297T>C (p.Tyr1099=) rs114593924 0.00538
NM_001166108.2(PALLD):c.2442A>G (p.Thr814=) rs113676921 0.00447
NM_001166108.2(PALLD):c.*492A>G rs113794451 0.00208
NM_001166108.2(PALLD):c.*946C>A rs76997292 0.00154
NM_001166108.2(PALLD):c.3256C>T (p.Leu1086=) rs59633770 0.00138
NM_001166108.2(PALLD):c.*1594T>C rs148023504 0.00102
NM_001166108.2(PALLD):c.2393T>C (p.Met798Thr) rs142116575 0.00102
NM_001166108.2(PALLD):c.33-4G>A rs113515140 0.00094
NM_001166108.2(PALLD):c.*1808C>T rs539762995 0.00089
NM_001166108.2(PALLD):c.*2141A>G rs962914167 0.00071
NM_001166108.2(PALLD):c.*1792T>A rs186567215 0.00070
NM_001166108.2(PALLD):c.2199+8G>A rs200060953 0.00070
NM_001166108.2(PALLD):c.*2027T>C rs192990293 0.00063
NM_001166108.2(PALLD):c.*1829T>C rs184106989 0.00046
NM_001166108.2(PALLD):c.*1131T>G rs773353973 0.00023
NM_001166108.2(PALLD):c.*2184G>A rs769635594 0.00019
NM_001166108.2(PALLD):c.*994A>G rs185646548 0.00019
NM_001166108.2(PALLD):c.2197C>G (p.Gln733Glu) rs140360991 0.00019
NM_001166108.2(PALLD):c.*2171T>C rs548951283 0.00015
NM_001166108.2(PALLD):c.2784T>C (p.Pro928=) rs114250766 0.00010
NM_001166108.2(PALLD):c.*908A>G rs886059212 0.00007
NM_001166108.2(PALLD):c.*108C>T rs863224704 0.00005
NM_001166108.2(PALLD):c.*2070G>C rs886059217 0.00005
NM_001166108.2(PALLD):c.*439T>C rs972893704 0.00005
NM_001166108.2(PALLD):c.*2022A>G rs886059216 0.00004
NM_001166108.2(PALLD):c.*1655A>T rs976050795 0.00003
NM_001166108.2(PALLD):c.*1713T>C rs765552955 0.00002
NM_001166108.2(PALLD):c.*2166A>G rs886059220 0.00002
NM_001166108.2(PALLD):c.*400T>C rs748402946 0.00002
NM_001166108.2(PALLD):c.2891A>C (p.Asp964Ala) rs750112132 0.00002
NM_001166108.2(PALLD):c.3052G>A (p.Val1018Ile) rs764754301 0.00002
NM_001166108.2(PALLD):c.*1787T>C rs886059215 0.00001
NM_001166108.2(PALLD):c.*2214C>T rs145960760 0.00001
NM_001166108.2(PALLD):c.*386T>C rs575876255 0.00001
NM_001166108.2(PALLD):c.2112C>T (p.Tyr704=) rs372414187 0.00001
NM_001166108.2(PALLD):c.2539C>G (p.Leu847Val) rs544491953 0.00001
NM_001166108.2(PALLD):c.2627G>A (p.Arg876His) rs115274645 0.00001
NM_001166108.2(PALLD):c.2867C>T (p.Thr956Ile) rs371498362 0.00001
NM_001166108.2(PALLD):c.2906G>A (p.Arg969His) rs769973229 0.00001
NM_001166108.2(PALLD):c.3087T>A (p.Phe1029Leu) rs189021816 0.00001
NM_001166108.2(PALLD):c.3352G>A (p.Val1118Ile) rs781065277 0.00001
NM_001166108.2(PALLD):c.*1132T>C rs575893643
NM_001166108.2(PALLD):c.*1757T>G rs886059214
NM_001166108.2(PALLD):c.*2168C>A rs886059221
NM_001166108.2(PALLD):c.*461G>A rs939786378
NM_001166108.2(PALLD):c.2297A>G (p.Glu766Gly)
NM_001166108.2(PALLD):c.2686C>T (p.Arg896Trp) rs772889018
NM_001166108.2(PALLD):c.3050T>C (p.Val1017Ala) rs1560929667
NM_001166108.2(PALLD):c.3080_3081del (p.Pro1027fs)
NM_001166108.2(PALLD):c.3150A>G (p.Val1050=) rs781516286

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.