ClinVar Miner

List of variants in gene DSP reported as likely benign for not provided

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Gene type:
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Total variants: 44
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HGVS dbSNP
NM_004415.4(DSP):c.*9T>A rs11558732
NM_004415.4(DSP):c.-32G>T
NM_004415.4(DSP):c.157T>G (p.Ser53Ala) rs397516918
NM_004415.4(DSP):c.170+235G>A
NM_004415.4(DSP):c.1778A>G (p.Asn593Ser) rs34239595
NM_004415.4(DSP):c.2037A>G (p.Ile679Met) rs151049942
NM_004415.4(DSP):c.2360A>C (p.Tyr787Ser) rs778350289
NM_004415.4(DSP):c.2596C>T (p.Arg866Cys) rs142429411
NM_004415.4(DSP):c.2630+237C>T
NM_004415.4(DSP):c.2723G>A (p.Arg908His) rs142494121
NM_004415.4(DSP):c.273+11C>G
NM_004415.4(DSP):c.2986-42T>A
NM_004415.4(DSP):c.3297G>C (p.Lys1099Asn) rs370550974
NM_004415.4(DSP):c.3701A>G (p.Asn1234Ser) rs185367490
NM_004415.4(DSP):c.3981C>T (p.Ile1327=) rs397516934
NM_004415.4(DSP):c.4005G>A (p.Gln1335=)
NM_004415.4(DSP):c.4034A>C (p.Glu1345Ala) rs201964660
NM_004415.4(DSP):c.4141A>T (p.Thr1381Ser) rs77758574
NM_004415.4(DSP):c.4372C>G (p.Arg1458Gly) rs28763965
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.4741A>G (p.Lys1581Glu) rs186842903
NM_004415.4(DSP):c.4750G>A (p.Ala1584Thr) rs191778417
NM_004415.4(DSP):c.5167G>C (p.Glu1723Gln) rs142803672
NM_004415.4(DSP):c.5178C>A (p.Asn1726Lys) rs147415451
NM_004415.4(DSP):c.5218G>A (p.Glu1740Lys) rs142885240
NM_004415.4(DSP):c.531C>G (p.Gly177=) rs138865799
NM_004415.4(DSP):c.55C>A (p.Arg19Ser)
NM_004415.4(DSP):c.597+102G>C
NM_004415.4(DSP):c.597+306G>A
NM_004415.4(DSP):c.6208G>A (p.Asp2070Asn) rs41302885
NM_004415.4(DSP):c.6799A>T (p.Thr2267Ser) rs181378432
NM_004415.4(DSP):c.688G>A (p.Asp230Asn) rs147315869
NM_004415.4(DSP):c.726+234T>C
NM_004415.4(DSP):c.726+43C>T
NM_004415.4(DSP):c.727-296G>A
NM_004415.4(DSP):c.778-224C>T
NM_004415.4(DSP):c.778-263A>T
NM_004415.4(DSP):c.782C>T (p.Ala261Val) rs139509870
NM_004415.4(DSP):c.7916G>A (p.Arg2639Gln) rs116888866
NM_004415.4(DSP):c.8191T>C (p.Tyr2731His) rs201397978
NM_004415.4(DSP):c.8455A>C (p.Met2819Leu) rs138329459
NM_004415.4(DSP):c.8467C>G (p.Pro2823Ala) rs142717240
NM_004415.4(DSP):c.940-292G>A

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