ClinVar Miner

List of variants in gene DSP reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP
NM_004415.2(DSP):c.*9T>A rs11558732
NM_004415.2(DSP):c.105G>A (p.Gly35=) rs77445784
NM_004415.2(DSP):c.1206G>A (p.Lys402=) rs150422458
NM_004415.2(DSP):c.1266+6G>T rs73375345
NM_004415.2(DSP):c.126T>C (p.Tyr42=) rs36087964
NM_004415.2(DSP):c.12C>G (p.Asn4Lys) rs368802003
NM_004415.2(DSP):c.1344G>A (p.Leu448=) rs138226280
NM_004415.2(DSP):c.1481A>T (p.Tyr494Phe) rs28763961
NM_004415.2(DSP):c.1488G>A (p.Thr496=) rs35820473
NM_004415.2(DSP):c.1920C>T (p.Ile640=) rs74806300
NM_004415.2(DSP):c.1dupA (p.Met1Asnfs) rs17133512
NM_004415.2(DSP):c.2631G>A (p.Arg877=) rs1016835
NM_004415.2(DSP):c.2673T>C (p.Tyr891=) rs146407262
NM_004415.2(DSP):c.2723G>A (p.Arg908His) rs142494121
NM_004415.2(DSP):c.2815G>A (p.Gly939Ser) rs80325569
NM_004415.2(DSP):c.2862C>T (p.Cys954=) rs2064217
NM_004415.2(DSP):c.2986-6T>A rs144748036
NM_004415.2(DSP):c.3018A>G (p.Leu1006=) rs375412541
NM_004415.2(DSP):c.3510G>A (p.Glu1170=) rs28763964
NM_004415.2(DSP):c.3696C>A (p.Ser1232=) rs141120358
NM_004415.2(DSP):c.3963G>A (p.Gln1321=) rs61731476
NM_004415.2(DSP):c.4065T>C (p.Tyr1355=) rs148478829
NM_004415.2(DSP):c.4141A>T (p.Thr1381Ser) rs77758574
NM_004415.2(DSP):c.4383G>A (p.Glu1461=) rs140029036
NM_004415.2(DSP):c.4455G>T (p.Arg1485Ser) rs113902911
NM_004415.2(DSP):c.4489C>T (p.Arg1497Trp) rs148041814
NM_004415.2(DSP):c.4535A>G (p.Tyr1512Cys) rs2076299
NM_004415.2(DSP):c.4578C>A (p.Asn1526Lys) rs28763966
NM_004415.2(DSP):c.4588G>T (p.Val1530Phe) rs141227126
NM_004415.2(DSP):c.4609C>T (p.Arg1537Cys) rs28763967
NM_004415.2(DSP):c.4741A>G (p.Lys1581Glu) rs186842903
NM_004415.2(DSP):c.4773G>A (p.Arg1591=) rs28763968
NM_004415.2(DSP):c.5213G>A (p.Arg1738Gln) rs6929069
NM_004415.2(DSP):c.522T>C (p.Cys174=) rs144781697
NM_004415.2(DSP):c.5498A>T (p.Glu1833Val) rs78652302
NM_004415.2(DSP):c.6390T>C (p.Ala2130=) rs28763969
NM_004415.2(DSP):c.7122C>T (p.Thr2374=) rs2076300
NM_004415.2(DSP):c.7734C>T (p.Ser2578=) rs28763970
NM_004415.2(DSP):c.7916G>A (p.Arg2639Gln) rs116888866
NM_004415.2(DSP):c.7995G>A (p.Thr2665=) rs35379048
NM_004415.2(DSP):c.8019C>T (p.Asp2673=) rs144275591
NM_004415.2(DSP):c.8175C>A (p.Arg2725=) rs11558731
NM_004415.2(DSP):c.8191T>C (p.Tyr2731His) rs201397978
NM_004415.2(DSP):c.8268A>C (p.Ile2756=) rs397516963
NM_004415.2(DSP):c.8300C>A (p.Thr2767Asn) rs34884895
NM_004415.2(DSP):c.8301C>G (p.Thr2767=) rs145362059
NM_004415.2(DSP):c.8455A>C (p.Met2819Leu) rs138329459
NM_004415.2(DSP):c.8472G>C (p.Gly2824=) rs2744380
NM_004415.2(DSP):c.8481C>T (p.Ser2827=) rs151029175
NM_004415.2(DSP):c.8605A>G (p.Ile2869Val) rs28763971
NM_004415.2(DSP):c.913A>T (p.Ile305Phe) rs17604693
NM_004415.3(DSP):c.1141-44C>T rs2076296
NM_004415.3(DSP):c.1903+7T>C rs28763962
NM_004415.3(DSP):c.1904-49T>A rs2076303
NM_004415.3(DSP):c.2091A= (p.Gly697=) rs2076304
NM_004415.3(DSP):c.2091A>G (p.Gly697=) rs2076304
NM_004415.3(DSP):c.237C>T (p.Ser79=) rs146521568
NM_004415.3(DSP):c.2437-11del rs727502998
NM_004415.3(DSP):c.2630+18C>T rs145963404
NM_004415.3(DSP):c.2631G= (p.Arg877=) rs1016835
NM_004415.3(DSP):c.273+10C>T rs56148603
NM_004415.3(DSP):c.274-31T>C rs10484326
NM_004415.3(DSP):c.3084+24T>G rs2806229
NM_004415.3(DSP):c.3084+28G>A rs2842691
NM_004415.3(DSP):c.3923G>A (p.Arg1308Gln) rs184154918
NM_004415.3(DSP):c.423-16_423-15insC rs113028223
NM_004415.3(DSP):c.6192T>C (p.Asn2064=) rs371230455
NM_004415.3(DSP):c.6208G>A (p.Asp2070Asn) rs41302885
NM_004415.3(DSP):c.6381C>T (p.Ala2127=) rs146315412
NM_004415.3(DSP):c.6753G>A (p.Lys2251=) rs750294829
NM_004415.3(DSP):c.741G>A (p.Ala247=) rs2806234
NM_004415.3(DSP):c.8472G= (p.Gly2824=) rs2744380

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