ClinVar Miner

List of variants in gene SPOP reported as likely pathogenic for adenocarcinoma

Included ClinVar conditions (108):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001007228.2(SPOP):c.259T>A (p.Tyr87Asn) rs1057519972
NM_001007228.2(SPOP):c.260A>C (p.Tyr87Ser) rs1057519971
NM_001007228.2(SPOP):c.260A>G (p.Tyr87Cys) rs1057519971
NM_001007228.2(SPOP):c.304T>G (p.Phe102Val) rs1057519964
NM_001007228.2(SPOP):c.305T>G (p.Phe102Cys) rs193920894
NM_001007228.2(SPOP):c.306C>G (p.Phe102Leu) rs1057519965
NM_001007228.2(SPOP):c.391T>A (p.Trp131Arg) rs1057519968
NM_001007228.2(SPOP):c.391T>G (p.Trp131Gly) rs1057519968
NM_001007228.2(SPOP):c.392G>C (p.Trp131Ser) rs1057519969
NM_001007228.2(SPOP):c.393G>T (p.Trp131Cys) rs1057519970
NM_001007228.2(SPOP):c.397T>A (p.Phe133Ile) rs1057519966
NM_001007228.2(SPOP):c.397T>G (p.Phe133Val) rs1057519966
NM_001007228.2(SPOP):c.398T>C (p.Phe133Ser) rs1057519967
NM_001007228.2(SPOP):c.398T>G (p.Phe133Cys) rs1057519967
NM_001007228.2(SPOP):c.399C>G (p.Phe133Leu) rs193921065

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