ClinVar Miner

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

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP
NM_007214.4(SEC63):c.*3959dupT rs112734053
NM_007214.4(SEC63):c.340-12_340-10delGTT rs200904488
NM_007214.4(SEC63):c.340-12_340-11delGT rs139413431
NM_007214.4(SEC63):c.340-12_340-8delGTTTT rs747514864
NM_007214.4(SEC63):c.340-9_340-7delTTT rs66526324
NM_007214.5(SEC63):c.*123T>A rs503068
NM_007214.5(SEC63):c.*1398A>C rs556907
NM_007214.5(SEC63):c.*1526T>C rs557911
NM_007214.5(SEC63):c.*1705G>A rs672444
NM_007214.5(SEC63):c.*1790_*1793del rs150602806
NM_007214.5(SEC63):c.*1901A>G rs10872020
NM_007214.5(SEC63):c.*1926_*1931del rs55885857
NM_007214.5(SEC63):c.*2504dup rs113337131
NM_007214.5(SEC63):c.*2662G>A rs513325
NM_007214.5(SEC63):c.*2705T>C rs687374
NM_007214.5(SEC63):c.*2811C>T rs74799313
NM_007214.5(SEC63):c.*3334C>T rs112894937
NM_007214.5(SEC63):c.*3393C>T rs592939
NM_007214.5(SEC63):c.*3431A>C rs592989
NM_007214.5(SEC63):c.*3480del rs56104837
NM_007214.5(SEC63):c.*3497A>G rs6933329
NM_007214.5(SEC63):c.*3574_*3575insGAC rs10685655
NM_007214.5(SEC63):c.*3580G>A rs847120
NM_007214.5(SEC63):c.-77C>T rs2272884
NM_007214.5(SEC63):c.1936-7_1936-5dup rs766716921
NM_007214.5(SEC63):c.340-12del rs58827902
NM_007214.5(SEC63):c.564C>T (p.Asn188=) rs675117

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