ClinVar Miner

List of variants in gene DSP reported as benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
NM_004415.2:c.2091A>G
NM_004415.2:c.741T>G
NM_004415.4(DSP):c.126T>C (p.Tyr42=) rs36087964
NM_004415.4(DSP):c.12C>G (p.Asn4Lys) rs368802003
NM_004415.4(DSP):c.1481A>T (p.Tyr494Phe) rs28763961
NM_004415.4(DSP):c.1dup (p.Met1fs) rs17133512
NM_004415.4(DSP):c.2631G>A (p.Arg877=) rs1016835
NM_004415.4(DSP):c.2815G>A (p.Gly939Ser) rs80325569
NM_004415.4(DSP):c.2862C>T (p.Cys954=) rs2064217
NM_004415.4(DSP):c.3510G>A (p.Glu1170=) rs28763964
NM_004415.4(DSP):c.3923G>A (p.Arg1308Gln) rs184154918
NM_004415.4(DSP):c.3963G>A (p.Gln1321=) rs61731476
NM_004415.4(DSP):c.4455G>T (p.Arg1485Ser) rs113902911
NM_004415.4(DSP):c.4535A>G (p.Tyr1512Cys) rs2076299
NM_004415.4(DSP):c.4578C>A (p.Asn1526Lys) rs28763966
NM_004415.4(DSP):c.4588G>T (p.Val1530Phe) rs141227126
NM_004415.4(DSP):c.4609C>T (p.Arg1537Cys) rs28763967
NM_004415.4(DSP):c.4773G>A (p.Arg1591=) rs28763968
NM_004415.4(DSP):c.5213G>A (p.Arg1738Gln) rs6929069
NM_004415.4(DSP):c.5498A>T (p.Glu1833Val) rs78652302
NM_004415.4(DSP):c.6390T>C (p.Ala2130=) rs28763969
NM_004415.4(DSP):c.688G>A (p.Asp230Asn) rs147315869
NM_004415.4(DSP):c.7122C>T (p.Thr2374=) rs2076300
NM_004415.4(DSP):c.7916G>A (p.Arg2639Gln) rs116888866
NM_004415.4(DSP):c.8175C>A (p.Arg2725=) rs11558731
NM_004415.4(DSP):c.8455A>C (p.Met2819Leu) rs138329459
NM_004415.4(DSP):c.8472G>C (p.Gly2824=) rs2744380
NM_004415.4(DSP):c.8605A>G (p.Ile2869Val) rs28763971
NM_004415.4(DSP):c.913A>T (p.Ile305Phe) rs17604693

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