ClinVar Miner

List of variants in gene SEC63 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
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HGVS dbSNP
NM_007214.4(SEC63):c.-264T>C rs565275212
NM_007214.4(SEC63):c.-268C>A rs565916525
NM_007214.5(SEC63):c.*1108A>G rs560882192
NM_007214.5(SEC63):c.*129G>A rs552904217
NM_007214.5(SEC63):c.*1612T>C rs76842245
NM_007214.5(SEC63):c.*1685A>C rs558069212
NM_007214.5(SEC63):c.*1839C>G rs150031834
NM_007214.5(SEC63):c.*1936del rs535127807
NM_007214.5(SEC63):c.*2046C>G rs139373195
NM_007214.5(SEC63):c.*2086G>C rs550478845
NM_007214.5(SEC63):c.*2376A>T rs78776458
NM_007214.5(SEC63):c.*2456G>A rs151325651
NM_007214.5(SEC63):c.*2479dup rs200116970
NM_007214.5(SEC63):c.*256T>C rs111637159
NM_007214.5(SEC63):c.*257A>G rs148053936
NM_007214.5(SEC63):c.*2607G>C rs549810875
NM_007214.5(SEC63):c.*2624T>C rs368337970
NM_007214.5(SEC63):c.*2886A>C rs182441835
NM_007214.5(SEC63):c.*3127C>T rs541730962
NM_007214.5(SEC63):c.*3128G>A rs114322175
NM_007214.5(SEC63):c.*3170C>T rs12529777
NM_007214.5(SEC63):c.*3210C>T rs570848637
NM_007214.5(SEC63):c.*3469T>G rs540628373
NM_007214.5(SEC63):c.*3498C>T rs577860076
NM_007214.5(SEC63):c.*3499A>C rs143966094
NM_007214.5(SEC63):c.*3501A>G rs377612532
NM_007214.5(SEC63):c.*3502C>T rs181941841
NM_007214.5(SEC63):c.*358T>C rs529945456
NM_007214.5(SEC63):c.*3704C>G rs554141897
NM_007214.5(SEC63):c.*3895T>C rs12661966
NM_007214.5(SEC63):c.*396T>A rs368205255
NM_007214.5(SEC63):c.*411C>T rs140498555
NM_007214.5(SEC63):c.*861A>G rs9480810
NM_007214.5(SEC63):c.*907C>T rs571893658
NM_007214.5(SEC63):c.1176G>A (p.Glu392=) rs61754483
NM_007214.5(SEC63):c.125-13del rs565329945
NM_007214.5(SEC63):c.1278C>T (p.Phe426=) rs146559698
NM_007214.5(SEC63):c.1441-5C>T rs370312823
NM_007214.5(SEC63):c.1625_1626insTAC (p.Gln543_Ser544insThr) rs779139584
NM_007214.5(SEC63):c.1666G>A (p.Val556Ile) rs17854547
NM_007214.5(SEC63):c.1674T>C (p.Asn558=) rs143570743
NM_007214.5(SEC63):c.1697_1699AAG[2] (p.Glu568del) rs752018806
NM_007214.5(SEC63):c.1936-4_1936-3insTT rs773608064
NM_007214.5(SEC63):c.2027C>T (p.Thr676Ile) rs61733388
NM_007214.5(SEC63):c.2134T>C (p.Leu712=) rs61733387
NM_007214.5(SEC63):c.230T>C (p.Ile77Thr) rs140251976
NM_007214.5(SEC63):c.340-15_340-13del rs150022935
NM_007214.5(SEC63):c.340-6_340-5dup rs142388422
NM_007214.5(SEC63):c.807G>A (p.Thr269=) rs182467867

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