ClinVar Miner

List of variants in gene CLDN16 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP
NM_001378492.1(CLDN16):c.-93-272C>T
NM_001378492.1(CLDN16):c.-93-323G>T
NM_006580.3(CLDN16):c.*1170G>A rs886058250
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.*1491A>G rs113286536
NM_006580.3(CLDN16):c.*1559C>A rs886058253
NM_006580.3(CLDN16):c.*1733A>G rs886058254
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.*768del rs886058249
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.227A>C (p.Gln76Pro) rs867514971
NM_006580.3(CLDN16):c.324+13C>G rs369250510
NM_006580.3(CLDN16):c.327G>A (p.Val109=) rs528344809
NM_006580.3(CLDN16):c.38del (p.Leu13fs) rs886058244
NM_006580.3(CLDN16):c.880G>A (p.Glu294Lys) rs756192568
NM_006580.4(CLDN16):c.*1427A>G
NM_006580.4(CLDN16):c.*1552T>G
NM_006580.4(CLDN16):c.*1793G>C
NM_006580.4(CLDN16):c.*1817T>C
NM_006580.4(CLDN16):c.*1872C>A
NM_006580.4(CLDN16):c.*1883T>G
NM_006580.4(CLDN16):c.*2014T>C
NM_006580.4(CLDN16):c.*299A>G
NM_006580.4(CLDN16):c.*493T>C
NM_006580.4(CLDN16):c.*495A>T
NM_006580.4(CLDN16):c.*541A>G
NM_006580.4(CLDN16):c.*586G>T
NM_006580.4(CLDN16):c.*769A>C
NM_006580.4(CLDN16):c.-116G>T
NM_006580.4(CLDN16):c.-132G>A
NM_006580.4(CLDN16):c.192C>T (p.Tyr64=)
NM_006580.4(CLDN16):c.22A>G (p.Ile8Val)
NM_006580.4(CLDN16):c.539G>C (p.Gly180Ala)
NM_006580.4(CLDN16):c.564T>C (p.Tyr188=)
NM_006580.4(CLDN16):c.575-7C>T
NM_006580.4(CLDN16):c.596A>G (p.Tyr199Cys)
NM_006580.4(CLDN16):c.628G>A (p.Ala210Thr)
NM_006580.4(CLDN16):c.99T>C (p.Ala33=)

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