ClinVar Miner

List of variants in gene UPF3B reported as likely benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_080632.2(UPF3B):c.*40G>A rs199925511
NM_080632.2(UPF3B):c.*49C>T rs182885401
NM_080632.2(UPF3B):c.*725G>A rs146388339
NM_080632.2(UPF3B):c.-100G>A rs769093842
NM_080632.2(UPF3B):c.-13G>C rs185511642
NM_080632.2(UPF3B):c.-67T>G rs761175084
NM_080632.2(UPF3B):c.1121G>A (p.Arg374His) rs143538947
NM_080632.3(UPF3B):c.1101G>C (p.Lys367Asn) rs199727706

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