ClinVar Miner

List of variants in gene CD46 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: 47
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HGVS dbSNP
NM_172351.3(CD46):c.*1099A>G rs886045842
NM_172351.3(CD46):c.*1111C>G rs193023975
NM_172351.3(CD46):c.*1146G>C
NM_172351.3(CD46):c.*1211C>T
NM_172351.3(CD46):c.*1265T>C
NM_172351.3(CD46):c.*1272C>T
NM_172351.3(CD46):c.*1418T>C
NM_172351.3(CD46):c.*1613C>T
NM_172351.3(CD46):c.*1614G>A
NM_172351.3(CD46):c.*1641A>G rs886045843
NM_172351.3(CD46):c.*1659A>G rs886045844
NM_172351.3(CD46):c.*1665G>A rs886045845
NM_172351.3(CD46):c.*180T>C rs886045840
NM_172351.3(CD46):c.*1865G>C
NM_172351.3(CD46):c.*1888C>T rs886045846
NM_172351.3(CD46):c.*1963C>T rs886045847
NM_172351.3(CD46):c.*31A>G rs886045839
NM_172351.3(CD46):c.*467T>C
NM_172351.3(CD46):c.*517T>A rs539666226
NM_172351.3(CD46):c.*518A>G
NM_172351.3(CD46):c.*52G>A rs373138507
NM_172351.3(CD46):c.*614T>C rs561506830
NM_172351.3(CD46):c.*672A>T
NM_172351.3(CD46):c.*920A>G rs886045841
NM_172351.3(CD46):c.*968T>A rs768037862
NM_172351.3(CD46):c.-10C>T
NM_172351.3(CD46):c.-127A>G
NM_172351.3(CD46):c.-6C>T rs886045836
NM_172351.3(CD46):c.1013C>T (p.Ala338Val) rs35366573
NM_172351.3(CD46):c.1018+7A>G
NM_172351.3(CD46):c.101C>T (p.Ala34Val)
NM_172351.3(CD46):c.1082+13A>T
NM_172351.3(CD46):c.1090C>T (p.Leu364=)
NM_172351.3(CD46):c.1104C>T (p.Thr368=)
NM_172351.3(CD46):c.118A>G (p.Thr40Ala) rs753924720
NM_172351.3(CD46):c.245G>A (p.Arg82Gln)
NM_172351.3(CD46):c.276C>T (p.Asp92=) rs148383499
NM_172351.3(CD46):c.285T>C (p.Tyr95=)
NM_172351.3(CD46):c.293C>T (p.Thr98Ile)
NM_172351.3(CD46):c.574G>C (p.Asp192His) rs368371683
NM_172351.3(CD46):c.586G>C (p.Gly196Arg)
NM_172351.3(CD46):c.857-124T>A rs886045837
NM_172351.3(CD46):c.857-185T>C
NM_172351.3(CD46):c.860C>T (p.Ser287Leu) rs751860518
NM_172351.3(CD46):c.887C>T (p.Ala296Val) rs753859532
NM_172351.3(CD46):c.901+9A>G rs370112627
NM_172351.3(CD46):c.949C>G (p.Pro317Ala) rs886045838

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