ClinVar Miner

List of variants in gene DSP reported as likely benign by Color

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Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP
NM_004415.2(DSP):c.1005A>G (p.Gln335=) rs200961741
NM_004415.2(DSP):c.1045-8T>C rs201633815
NM_004415.2(DSP):c.1206G>A (p.Lys402=) rs150422458
NM_004415.2(DSP):c.1344G>A (p.Leu448=) rs138226280
NM_004415.2(DSP):c.1483G>A (p.Val495Met) rs372014020
NM_004415.2(DSP):c.1488G>A (p.Thr496=) rs35820473
NM_004415.2(DSP):c.1695C>T (p.Ile565=) rs752714010
NM_004415.2(DSP):c.2121C>T (p.Asn707=) rs368590198
NM_004415.2(DSP):c.2346C>T (p.Asp782=) rs139071827
NM_004415.2(DSP):c.2422C>T (p.Arg808Cys) rs150339369
NM_004415.2(DSP):c.2723G>A (p.Arg908His) rs142494121
NM_004415.2(DSP):c.2773C>T (p.Arg925Trp) rs145933612
NM_004415.2(DSP):c.2986-6T>A rs144748036
NM_004415.2(DSP):c.3018A>G (p.Leu1006=) rs375412541
NM_004415.2(DSP):c.3102C>T (p.Ile1034=) rs569974617
NM_004415.2(DSP):c.3123C>T (p.Leu1041=) rs149929637
NM_004415.2(DSP):c.3303C>T (p.Tyr1101=) rs372440854
NM_004415.2(DSP):c.3507C>T (p.Tyr1169=) rs148894066
NM_004415.2(DSP):c.3650C>T (p.Thr1217Met) rs535202724
NM_004415.2(DSP):c.3701A>G (p.Asn1234Ser) rs185367490
NM_004415.2(DSP):c.4041A>G (p.Glu1347=) rs200671552
NM_004415.2(DSP):c.4065T>C (p.Tyr1355=) rs148478829
NM_004415.2(DSP):c.4320G>A (p.Val1440=) rs571103583
NM_004415.2(DSP):c.4372C>G (p.Arg1458Gly) rs28763965
NM_004415.2(DSP):c.4401A>G (p.Gln1467=) rs199818953
NM_004415.2(DSP):c.4515G>A (p.Ala1505=) rs193197554
NM_004415.2(DSP):c.4741A>G (p.Lys1581Glu) rs186842903
NM_004415.2(DSP):c.4750G>A (p.Ala1584Thr) rs191778417
NM_004415.2(DSP):c.4752G>A (p.Ala1584=) rs201213622
NM_004415.2(DSP):c.4943A>G (p.Gln1648Arg) rs202232360
NM_004415.2(DSP):c.5154G>A (p.Leu1718=) rs376620183
NM_004415.2(DSP):c.5178C>A (p.Asn1726Lys) rs147415451
NM_004415.2(DSP):c.5283C>T (p.Asn1761=) rs763355815
NM_004415.2(DSP):c.5523A>C (p.Ser1841=) rs730882116
NM_004415.2(DSP):c.5554C>T (p.Arg1852Cys) rs550818559
NM_004415.2(DSP):c.5593A>T (p.Asn1865Tyr) rs562015789
NM_004415.2(DSP):c.5913G>T (p.Leu1971=) rs373416071
NM_004415.2(DSP):c.6655G>A (p.Val2219Ile) rs397516953
NM_004415.2(DSP):c.6678T>A (p.Gly2226=) rs149070106
NM_004415.2(DSP):c.6927G>A (p.Arg2309=) rs747248981
NM_004415.2(DSP):c.7077C>T (p.Ile2359=) rs966841386
NM_004415.2(DSP):c.7125G>A (p.Gly2375=) rs141709096
NM_004415.2(DSP):c.7197G>A (p.Glu2399=) rs372594837
NM_004415.2(DSP):c.729C>T (p.Arg243=) rs141028505
NM_004415.2(DSP):c.8019C>T (p.Asp2673=) rs144275591
NM_004415.2(DSP):c.8415C>T (p.Ala2805=) rs377148997
NM_004415.2(DSP):c.88G>A (p.Val30Met) rs121912998
NM_004415.3(DSP):c.5218G>A (p.Glu1740Lys) rs142885240
NM_004415.3(DSP):c.5555G>A (p.Arg1852His) rs193922669
NM_004415.3(DSP):c.6208G>A (p.Asp2070Asn) rs41302885
NM_004415.3(DSP):c.6881C>G (p.Ala2294Gly) rs147000526
NM_004415.3(DSP):c.8529_8540delTGGGTCCCGGAG (p.Ser2843_Arg2846del) rs794728151
NM_004415.4(DSP):c.1266+6G>A
NM_004415.4(DSP):c.1329G>A (p.Lys443=)
NM_004415.4(DSP):c.2205T>C (p.Gly735=)
NM_004415.4(DSP):c.2568C>T (p.Phe856=)
NM_004415.4(DSP):c.277T>C (p.Leu93=)
NM_004415.4(DSP):c.3819C>T (p.Asn1273=)
NM_004415.4(DSP):c.4032T>C (p.Tyr1344=)
NM_004415.4(DSP):c.4350G>A (p.Glu1450=)
NM_004415.4(DSP):c.5205G>A (p.Arg1735=)
NM_004415.4(DSP):c.5380-15C>A
NM_004415.4(DSP):c.6373C>T (p.Leu2125=)
NM_004415.4(DSP):c.6549C>T (p.Tyr2183=)
NM_004415.4(DSP):c.6804A>G (p.Thr2268=)
NM_004415.4(DSP):c.6918C>T (p.Ser2306=)
NM_004415.4(DSP):c.7563T>C (p.Asp2521=)
NM_004415.4(DSP):c.778-6G>T
NM_004415.4(DSP):c.7854C>G (p.Pro2618=)
NM_004415.4(DSP):c.7983C>A (p.Ile2661=)
NM_004415.4(DSP):c.8300C>T (p.Thr2767Ile)

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