ClinVar Miner

List of variants in gene DSP reported as uncertain significance by Integrated Genetics/Laboratory Corporation of America

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Gene type:
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Total variants: 30
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HGVS dbSNP
NM_004415.4(DSP):c.1067C>A (p.Thr356Lys) rs780626687
NM_004415.4(DSP):c.163G>T (p.Gly55Cys) rs1214660308
NM_004415.4(DSP):c.1702-18C>T rs148417566
NM_004415.4(DSP):c.1997C>T (p.Thr666Ile) rs200053977
NM_004415.4(DSP):c.2415A>C (p.Glu805Asp) rs1554107530
NM_004415.4(DSP):c.2617C>G (p.Gln873Glu) rs794728118
NM_004415.4(DSP):c.2675G>A (p.Arg892His)
NM_004415.4(DSP):c.272C>T (p.Pro91Leu) rs1561679365
NM_004415.4(DSP):c.273+5G>A rs200473206
NM_004415.4(DSP):c.3462T>A (p.Gly1154=) rs1554108086
NM_004415.4(DSP):c.3492C>G (p.Ile1164Met) rs1561697488
NM_004415.4(DSP):c.4118C>T (p.Thr1373Ile) rs762930286
NM_004415.4(DSP):c.4466T>G (p.Leu1489Arg) rs746782582
NM_004415.4(DSP):c.4754C>T (p.Ser1585Leu) rs773622004
NM_004415.4(DSP):c.4775A>G (p.Lys1592Arg) rs200421954
NM_004415.4(DSP):c.4901G>A (p.Arg1634Gln) rs144106775
NM_004415.4(DSP):c.521G>T (p.Cys174Phe) rs377507763
NM_004415.4(DSP):c.5396A>G (p.Gln1799Arg) rs987386495
NM_004415.4(DSP):c.5412G>T (p.Gln1804His) rs779809935
NM_004415.4(DSP):c.5631T>C (p.Ala1877=) rs1231651139
NM_004415.4(DSP):c.5912T>C (p.Leu1971Pro) rs397516950
NM_004415.4(DSP):c.6247C>T (p.Arg2083Cys) rs370093129
NM_004415.4(DSP):c.6397G>A (p.Gly2133Ser) rs372393122
NM_004415.4(DSP):c.6566G>A (p.Arg2189Gln) rs766933370
NM_004415.4(DSP):c.6993T>C (p.Ser2331=) rs767282172
NM_004415.4(DSP):c.7583A>G (p.Tyr2528Cys) rs746932951
NM_004415.4(DSP):c.778-20C>T rs762596346
NM_004415.4(DSP):c.8117A>T (p.Lys2706Met) rs537588390
NM_004415.4(DSP):c.8493_8516del (p.2827_2830SGSR[3]) rs1554109280
NM_004415.4(DSP):c.946A>G (p.Met316Val) rs201672777

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