ClinVar Miner

List of variants in gene UPK3A reported as likely 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: 10
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HGVS dbSNP
NM_006953.4(UPK3A):c.-25G>C rs116162068
NM_006953.4(UPK3A):c.259T>G (p.Ser87Ala) rs145106685
NM_006953.4(UPK3A):c.260C>A (p.Ser87Ter) rs138918236
NM_006953.4(UPK3A):c.402C>T (p.Val134=) rs2673088
NM_006953.4(UPK3A):c.460G>C (p.Ala154Pro) rs1057353
NM_006953.4(UPK3A):c.465C>T (p.Pro155=) rs62001037
NM_006953.4(UPK3A):c.545G>A (p.Trp182Ter) rs147609981
NM_006953.4(UPK3A):c.549A>G (p.Ser183=) rs1135360
NM_006953.4(UPK3A):c.588G>A (p.Thr196=) rs115882180
NM_006953.4(UPK3A):c.858A>G (p.Gln286=) rs1057356

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