ClinVar Miner

List of variants in gene STIM1 reported as uncertain significance for not provided

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Total variants: 40
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HGVS dbSNP gnomAD frequency
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.458C>T (p.Thr153Ile) rs144602692 0.00022
NM_001382567.1(STIM1):c.454G>A (p.Glu152Lys) rs143916878 0.00013
NM_001382567.1(STIM1):c.792-8C>T rs201395930 0.00012
NM_001382567.1(STIM1):c.408G>C (p.Glu136Asp) rs200648767 0.00009
NM_001382567.1(STIM1):c.488C>A (p.Ala163Asp) rs199893056 0.00007
NM_001382567.1(STIM1):c.1394G>A (p.Arg465His) rs375914426 0.00005
NM_001382567.1(STIM1):c.1681C>T (p.Arg561Cys) rs142239530 0.00005
NM_001382567.1(STIM1):c.1765C>T (p.Arg589Trp) rs747547917 0.00005
NM_001382567.1(STIM1):c.1410C>G (p.His470Gln) rs748403696 0.00004
NM_001382567.1(STIM1):c.392A>G (p.Asn131Ser) rs201274425 0.00004
NM_001382567.1(STIM1):c.1382T>C (p.Met461Thr) rs1444907403 0.00003
NM_001382567.1(STIM1):c.1603A>G (p.Thr535Ala) rs200528072 0.00002
NM_001382567.1(STIM1):c.871A>G (p.Asn291Asp) rs201523207 0.00002
NM_001382567.1(STIM1):c.107C>T (p.Ser36Leu) rs200907515 0.00001
NM_001382567.1(STIM1):c.1439T>C (p.Met480Thr) rs762820296 0.00001
NM_001382567.1(STIM1):c.1634+249T>G rs1164304693 0.00001
NM_001382567.1(STIM1):c.1718G>A (p.Arg573His) rs202147687 0.00001
NM_001382567.1(STIM1):c.22G>A (p.Ala8Thr) rs751520286 0.00001
NM_001382567.1(STIM1):c.400G>A (p.Val134Met) rs200351944 0.00001
NM_001382567.1(STIM1):c.767A>G (p.Gln256Arg) rs201576757 0.00001
NM_001382567.1(STIM1):c.1299C>G (p.Ile433Met) rs200738706
NM_001382567.1(STIM1):c.1534G>A (p.Gly512Ser)
NM_001382567.1(STIM1):c.1634+166_1634+174del
NM_001382567.1(STIM1):c.1634+221C>G
NM_001382567.1(STIM1):c.1634+272C>G
NM_001382567.1(STIM1):c.1634+80T>A
NM_001382567.1(STIM1):c.1694C>T (p.Ala565Val) rs1382628661
NM_001382567.1(STIM1):c.1780G>T (p.Val594Phe)
NM_001382567.1(STIM1):c.2135A>G (p.Lys712Arg)
NM_001382567.1(STIM1):c.227A>G (p.Asp76Gly) rs2135736487
NM_001382567.1(STIM1):c.270+23215T>C
NM_001382567.1(STIM1):c.349G>A (p.Val117Met) rs759378488
NM_001382567.1(STIM1):c.541A>G (p.Met181Val) rs2094314118
NM_001382567.1(STIM1):c.643A>C (p.Met215Leu)
NM_001382567.1(STIM1):c.673G>T (p.Gly225Cys)
NM_001382567.1(STIM1):c.796C>T (p.His266Tyr) rs2133185569
NM_001382567.1(STIM1):c.970G>A (p.Val324Ile)
NM_001382567.1(STIM1):c.98G>C (p.Gly33Ala) rs2135170857

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