ClinVar Miner

List of variants in gene SPTB reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_001355436.2(SPTB):c.4618A>C (p.Arg1540=) rs61989884 0.00322
NM_001355436.2(SPTB):c.40C>T (p.Pro14Ser) rs147059670 0.00150
NM_001355436.2(SPTB):c.5651C>T (p.Ala1884Val) rs148337824 0.00150
NM_001355436.2(SPTB):c.6346-13dup rs555587693 0.00149
NM_001355436.2(SPTB):c.5750C>T (p.Ser1917Phe) rs149678681 0.00147
NM_001355436.2(SPTB):c.5050C>T (p.Arg1684Cys) rs141226650 0.00138
NM_001355436.2(SPTB):c.6496C>G (p.Pro2166Ala) rs144051169 0.00136
NM_001355436.2(SPTB):c.4670A>G (p.Glu1557Gly) rs140648376 0.00113
NM_001355436.2(SPTB):c.3015C>T (p.Ala1005=) rs147235045 0.00102
NM_001355436.2(SPTB):c.2060G>A (p.Arg687His) rs3742602 0.00101
NM_001355436.2(SPTB):c.3479G>A (p.Arg1160His) rs76283214 0.00048
NM_001355436.2(SPTB):c.2937C>T (p.Ser979=) rs141762497 0.00033
NM_001355436.2(SPTB):c.2480G>A (p.Arg827Gln) rs150013838 0.00028
NM_001355436.2(SPTB):c.1577C>T (p.Thr526Ile) rs145315673 0.00027
NM_001355436.2(SPTB):c.6484G>A (p.Glu2162Lys) rs375816870 0.00020
NM_001355436.2(SPTB):c.5943C>T (p.Arg1981=) rs75000411 0.00013
NM_001355436.2(SPTB):c.4511C>T (p.Ala1504Val) rs200876438 0.00011
NM_001355436.2(SPTB):c.4143C>T (p.Ser1381=) rs148504156 0.00008
NM_001355436.2(SPTB):c.2781G>A (p.Gln927=) rs368620488 0.00003
NM_001355436.2(SPTB):c.6132G>A (p.Val2044=) rs747360003 0.00001
NM_001355436.2(SPTB):c.1008C>T (p.Gly336=)
NM_001355436.2(SPTB):c.1059G>A (p.Pro353=)
NM_001355436.2(SPTB):c.1092T>C (p.Val364=)
NM_001355436.2(SPTB):c.1152C>T (p.His384=)
NM_001355436.2(SPTB):c.2214C>T (p.Asn738=)
NM_001355436.2(SPTB):c.2256G>A (p.Ala752=)
NM_001355436.2(SPTB):c.2946C>T (p.Asp982=)
NM_001355436.2(SPTB):c.2973C>T (p.Ile991=)
NM_001355436.2(SPTB):c.301-8_301-7insGG
NM_001355436.2(SPTB):c.3233C>T (p.Ser1078Phe)
NM_001355436.2(SPTB):c.3333C>T (p.Asp1111=)
NM_001355436.2(SPTB):c.3334G>A (p.Gly1112Arg)
NM_001355436.2(SPTB):c.360C>T (p.Leu120=) rs886038377
NM_001355436.2(SPTB):c.3768C>T (p.His1256=)
NM_001355436.2(SPTB):c.4320C>A (p.Ala1440=)
NM_001355436.2(SPTB):c.435G>T (p.Leu145=)
NM_001355436.2(SPTB):c.474+13G>A rs201559808
NM_001355436.2(SPTB):c.4812G>A (p.Glu1604=)
NM_001355436.2(SPTB):c.5211G>A (p.Arg1737=)
NM_001355436.2(SPTB):c.534G>A (p.Ala178=)
NM_001355436.2(SPTB):c.6393G>A (p.Pro2131=)
NM_001355436.2(SPTB):c.6498C>T (p.Pro2166=)
NM_001355436.2(SPTB):c.6518G>C (p.Arg2173Pro)
NM_001355436.2(SPTB):c.964A>G (p.Ile322Val)

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