ClinVar Miner

List of variants in gene CLDN16 studied for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP
CLDN16, LEU151PRO
NM_006580.3(CLDN16):c.*1117G>A rs10470534
NM_006580.3(CLDN16):c.*1170G>A rs886058250
NM_006580.3(CLDN16):c.*1178C>T rs533709248
NM_006580.3(CLDN16):c.*1313G>A rs565421878
NM_006580.3(CLDN16):c.*1333A>G rs886058251
NM_006580.3(CLDN16):c.*1348A>G rs753612393
NM_006580.3(CLDN16):c.*1377T>A rs886058252
NM_006580.3(CLDN16):c.*1453G>C rs13076274
NM_006580.3(CLDN16):c.*1491A>G rs113286536
NM_006580.3(CLDN16):c.*1559C>A rs886058253
NM_006580.3(CLDN16):c.*1733A>G rs886058254
NM_006580.3(CLDN16):c.*1763T>A rs9844654
NM_006580.3(CLDN16):c.*1779A>C rs115514339
NM_006580.3(CLDN16):c.*204C>T rs73053979
NM_006580.3(CLDN16):c.*2098T>G rs187708101
NM_006580.3(CLDN16):c.*243C>T rs142380851
NM_006580.3(CLDN16):c.*249G>A rs886058246
NM_006580.3(CLDN16):c.*724A>C rs886058247
NM_006580.3(CLDN16):c.*74A>G rs886058245
NM_006580.3(CLDN16):c.*761A>G rs886058248
NM_006580.3(CLDN16):c.*768delG rs886058249
NM_006580.3(CLDN16):c.*794T>C rs2293532
NM_006580.3(CLDN16):c.*842C>T rs77656241
NM_006580.3(CLDN16):c.*907A>G rs116488781
NM_006580.3(CLDN16):c.*965G>A rs769075597
NM_006580.3(CLDN16):c.-136T>C rs534883127
NM_006580.3(CLDN16):c.-3A>T rs200322099
NM_006580.3(CLDN16):c.-5G>A rs777259905
NM_006580.3(CLDN16):c.-6C>T rs557493885
NM_006580.3(CLDN16):c.-82A>G rs886058243
NM_006580.3(CLDN16):c.166G>C (p.Ala56Pro) rs3214506
NM_006580.3(CLDN16):c.166del (p.Ala56fs) rs368234054
NM_006580.3(CLDN16):c.212T>G (p.Met71Arg) rs104893724
NM_006580.3(CLDN16):c.227A>C (p.Gln76Pro) rs867514971
NM_006580.3(CLDN16):c.255C>G (p.Phe85Leu) rs149116671
NM_006580.3(CLDN16):c.324+10T>C rs1491994
NM_006580.3(CLDN16):c.324+13C>G rs369250510
NM_006580.3(CLDN16):c.327G>A (p.Val109=) rs528344809
NM_006580.3(CLDN16):c.350G>A (p.Trp117Ter) rs104893732
NM_006580.3(CLDN16):c.38del (p.Leu13fs) rs886058244
NM_006580.3(CLDN16):c.416C>T (p.Ala139Val) rs765256758
NM_006580.3(CLDN16):c.434T>C (p.Leu145Pro) rs104893731
NM_006580.3(CLDN16):c.445C>T (p.Arg149Ter) rs104893720
NM_006580.3(CLDN16):c.452T>G (p.Leu151Trp) rs104893730
NM_006580.3(CLDN16):c.453G>T (p.Leu151Phe) rs104893729
NM_006580.3(CLDN16):c.500T>C (p.Leu167Pro) rs104893725
NM_006580.3(CLDN16):c.545_548dup (p.Lys183delinsAsnTer) rs1253995767
NM_006580.3(CLDN16):c.571G>A (p.Gly191Arg) rs104893722
NM_006580.3(CLDN16):c.593G>A (p.Gly198Asp) rs104893723
NM_006580.3(CLDN16):c.602G>A (p.Gly201Glu)
NM_006580.3(CLDN16):c.678del (p.Gly227fs) rs1553809654
NM_006580.3(CLDN16):c.695T>G (p.Phe232Cys) rs104893726
NM_006580.3(CLDN16):c.698G>A (p.Gly233Asp) rs104893727
NM_006580.3(CLDN16):c.704C>T (p.Ser235Phe) rs104893728
NM_006580.3(CLDN16):c.715G>A (p.Gly239Arg) rs104893721
NM_006580.3(CLDN16):c.823A>T (p.Lys275Ter) rs387906880
NM_006580.3(CLDN16):c.830A>G (p.Tyr277Cys) rs35041121
NM_006580.3(CLDN16):c.831T>G (p.Tyr277Ter) rs121908543
NM_006580.3(CLDN16):c.880G>A (p.Glu294Lys) rs756192568

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