ClinVar Miner

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

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Total variants: 46
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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.*1906G>A rs1136603 0.13125
NM_001166108.2(PALLD):c.2679A>G (p.Arg893=) rs1059444 0.12743
NM_001166108.2(PALLD):c.3359-4G>A rs112116419 0.01852
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 0.00564
NM_001166108.2(PALLD):c.*492A>G rs113794451 0.00224
NM_001166108.2(PALLD):c.2442A>G (p.Thr814=) rs113676921 0.00218
NM_001166108.2(PALLD):c.33-4G>A rs113515140 0.00105
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.3256C>T (p.Leu1086=) rs59633770 0.00098
NM_001166108.2(PALLD):c.*946C>A rs76997292 0.00096
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 0.00065
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 0.00020
NM_001166108.2(PALLD):c.*2171T>C rs548951283 0.00014
NM_001166108.2(PALLD):c.*994A>G rs185646548 0.00014
NM_001166108.2(PALLD):c.2784T>C (p.Pro928=) rs114250766 0.00010
NM_001166108.2(PALLD):c.*2070G>C rs886059217 0.00006
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.*1808C>T rs539762995 0.00003
NM_001166108.2(PALLD):c.*908A>G rs886059212 0.00003
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.*1787T>C rs886059215 0.00001
NM_001166108.2(PALLD):c.*2166A>G rs886059220 0.00001
NM_001166108.2(PALLD):c.*2214C>T rs145960760 0.00001
NM_001166108.2(PALLD):c.2112C>T (p.Tyr704=) rs372414187 0.00001
NM_001166108.2(PALLD):c.2867C>T (p.Thr956Ile) rs371498362 0.00001
NM_001166108.2(PALLD):c.*1132T>C rs575893643
NM_001166108.2(PALLD):c.*1713T>C rs765552955
NM_001166108.2(PALLD):c.*1757T>G rs886059214
NM_001166108.2(PALLD):c.*2168C>A rs886059221
NM_001166108.2(PALLD):c.*386T>C rs575876255
NM_001166108.2(PALLD):c.*461G>A rs939786378
NM_001166108.2(PALLD):c.2686C>T (p.Arg896Trp) rs772889018
NM_001166108.2(PALLD):c.3150A>G (p.Val1050=) rs781516286

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