ClinVar Miner

List of variants in gene STT3B studied for congenital disorder of glycosylation type I

Included ClinVar conditions (31):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_178862.3(STT3B):c.1539+20G>T rs587777217
NM_178862.3(STT3B):c.1764C>T (p.Tyr588=) rs34176522
NM_178862.3(STT3B):c.2366A>G (p.Asn789Ser)
NM_178862.3(STT3B):c.619A>G (p.Ile207Val) rs780102016
NM_178862.3(STT3B):c.758G>C (p.Cys253Ser)
NM_178862.3(STT3B):c.777+7T>G rs76400963
NM_178862.3(STT3B):c.895A>G (p.Ile299Val)

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