ClinVar Miner

List of variants in gene combination STX16, STX16-NPEPL1 reported as uncertain significance 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: 37
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HGVS dbSNP
NM_001001433.3(STX16):c.*1160G>A rs886056855
NM_001001433.3(STX16):c.*1203T>C rs886056856
NM_001001433.3(STX16):c.*1232A>G rs886056857
NM_001001433.3(STX16):c.*1378A>T rs750137163
NM_001001433.3(STX16):c.*1547C>G rs532426531
NM_001001433.3(STX16):c.*173C>G rs765639298
NM_001001433.3(STX16):c.*1746C>T rs886056858
NM_001001433.3(STX16):c.*1764C>T rs886056859
NM_001001433.3(STX16):c.*1898A>G rs886056860
NM_001001433.3(STX16):c.*2016G>T rs779563360
NM_001001433.3(STX16):c.*2137C>T rs886056861
NM_001001433.3(STX16):c.*2312G>A rs886056862
NM_001001433.3(STX16):c.*2347_*2348insAAA rs761666161
NM_001001433.3(STX16):c.*2348del rs886056863
NM_001001433.3(STX16):c.*2363_*2366dup rs10695175
NM_001001433.3(STX16):c.*2364_*2366dup rs10695175
NM_001001433.3(STX16):c.*2475T>C rs886056864
NM_001001433.3(STX16):c.*2496del rs886056865
NM_001001433.3(STX16):c.*2499C>T rs886056866
NM_001001433.3(STX16):c.*2594T>C rs886056867
NM_001001433.3(STX16):c.*270T>C rs886056850
NM_001001433.3(STX16):c.*2896A>G rs886056868
NM_001001433.3(STX16):c.*3093A>G rs886056869
NM_001001433.3(STX16):c.*436G>C rs886056851
NM_001001433.3(STX16):c.*441C>G rs886056852
NM_001001433.3(STX16):c.*56T>C rs886056849
NM_001001433.3(STX16):c.*952C>A rs886056854
NM_001001433.3(STX16):c.-377G>A rs886056845
NM_001001433.3(STX16):c.-409G>A rs886056844
NM_001001433.3(STX16):c.-465T>G rs886056843
NM_001001433.3(STX16):c.-673C>G rs886056842
NM_001001433.3(STX16):c.-693G>A rs149351460
NM_001001433.3(STX16):c.-707G>A rs886056841
NM_001001433.3(STX16):c.716A>G (p.Glu239Gly) rs202102691
NM_001001433.3(STX16):c.904A>G (p.Met302Val) rs886056846
NM_001001433.3(STX16):c.907C>G (p.Leu303Val) rs886056847
NM_001001433.3(STX16):c.912G>C (p.Val304=) rs886056848

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