ClinVar Miner

List of variants in gene STIM1 reported as likely benign for not provided

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Gene type:
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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001382567.1(STIM1):c.969+167T>C rs111991757 0.01235
NM_001382567.1(STIM1):c.792-59G>T rs146231947 0.00902
NM_001382567.1(STIM1):c.139+246A>C rs113897235 0.00833
NM_001382567.1(STIM1):c.*172A>G rs3750996 0.00619
NM_001382567.1(STIM1):c.861C>T (p.Arg287=) rs16929446 0.00556
NM_001382567.1(STIM1):c.1137+116T>C rs16929441 0.00430
NM_003156.4(STIM1):c.1541+504T>C rs79806392 0.00429
NM_001382567.1(STIM1):c.1239-13C>T rs115353673 0.00426
NM_001382567.1(STIM1):c.1302G>A (p.Glu434=) rs116837894 0.00426
NM_001382567.1(STIM1):c.1604C>T (p.Thr535Met) rs146873551 0.00267
NM_001382567.1(STIM1):c.1634+269C>G rs139558513 0.00229
NM_001382567.1(STIM1):c.1664C>T (p.Ser555Phe) rs141215990 0.00163
NM_001382567.1(STIM1):c.1634+287G>A rs562406813 0.00157
NM_001382567.1(STIM1):c.114C>G (p.Ala38=) rs150033189 0.00029
NM_001382567.1(STIM1):c.1128C>T (p.Ala376=) rs200375470 0.00020
NM_001382567.1(STIM1):c.201A>G (p.Ala67=) rs200194500 0.00015
NM_001382567.1(STIM1):c.105C>T (p.Ser35=) rs139540641 0.00012
NM_001382567.1(STIM1):c.1611A>G (p.Pro537=) rs199512211 0.00003
NM_001382567.1(STIM1):c.1305C>T (p.Ile435=) rs199801171 0.00001
NM_001382567.1(STIM1):c.567G>A (p.Lys189=) rs202109124 0.00001
NM_001382567.1(STIM1):c.1215A>G (p.Val405=)
NM_001382567.1(STIM1):c.1461C>T (p.Pro487=) rs751169800
NM_001382567.1(STIM1):c.1525A>C (p.Thr509Pro)
NM_001382567.1(STIM1):c.1634+13C>A
NM_001382567.1(STIM1):c.198G>A (p.Glu66=)
NM_001382567.1(STIM1):c.271-3C>T rs561797617
NM_001382567.1(STIM1):c.742T>C (p.Leu248=) rs748663206
NM_001382567.1(STIM1):c.791+75C>G

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