ClinVar Miner

List of variants in gene VIPAS39 reported as pathogenic for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_001193315.1(VIPAS39):c.1179+1G>A
NM_001193315.1(VIPAS39):c.1184G>A (p.Trp395Ter) rs1555364979
NM_001193315.1(VIPAS39):c.20del (p.Asp7fs)
NM_001193315.1(VIPAS39):c.2T>G (p.Met1Arg) rs267607172
NM_001193315.1(VIPAS39):c.535C>T (p.Gln179Ter) rs267607173
NM_001193315.1(VIPAS39):c.658C>T (p.Arg220Ter) rs200370925
NM_001193315.1(VIPAS39):c.749_753del (p.Thr250fs) rs794726653
NM_001193315.1(VIPAS39):c.871C>T (p.Gln291Ter) rs267607171

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