ClinVar Miner

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

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Gene type:
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Total variants: 64
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HGVS dbSNP
NC_000006.12:g.7541350G>A
NC_000006.12:g.7541378G>C
NC_000006.12:g.7567737C>T
NC_000006.12:g.7571793T>A
NC_000006.12:g.7578160_7578163del
NC_000006.12:g.7578586T>G
NC_000006.12:g.7578590G>A
NM_004415.4(DSP):c.1206G>A (p.Lys402=) rs150422458
NM_004415.4(DSP):c.1266+215G>T
NM_004415.4(DSP):c.1420-93C>T
NM_004415.4(DSP):c.1481A>T (p.Tyr494Phe) rs28763961
NM_004415.4(DSP):c.170+163C>T
NM_004415.4(DSP):c.170+300C>A
NM_004415.4(DSP):c.1701+167A>G
NM_004415.4(DSP):c.1701+186C>G
NM_004415.4(DSP):c.1702-289G>T
NM_004415.4(DSP):c.171-285A>G
NM_004415.4(DSP):c.171-315_171-314insTATT
NM_004415.4(DSP):c.1903+57G>A
NM_004415.4(DSP):c.2297+51T>C
NM_004415.4(DSP):c.2298-38T>C
NM_004415.4(DSP):c.2298-85C>T
NM_004415.4(DSP):c.2631-159G>A
NM_004415.4(DSP):c.264C>T (p.Ile88=) rs727502997
NM_004415.4(DSP):c.2673T>C (p.Tyr891=) rs146407262
NM_004415.4(DSP):c.273+180G>T
NM_004415.4(DSP):c.273+191A>G
NM_004415.4(DSP):c.274-285dup
NM_004415.4(DSP):c.274-309A>G
NM_004415.4(DSP):c.2794-113G>A
NM_004415.4(DSP):c.2815G>A (p.Gly939Ser) rs80325569
NM_004415.4(DSP):c.2877+79C>A
NM_004415.4(DSP):c.2878-268A>G
NM_004415.4(DSP):c.2985+224G>C
NM_004415.4(DSP):c.2985+70G>A
NM_004415.4(DSP):c.3084+175C>T
NM_004415.4(DSP):c.3085-114A>G
NM_004415.4(DSP):c.3085-115C>T
NM_004415.4(DSP):c.3085-145A>T
NM_004415.4(DSP):c.3085-197G>T
NM_004415.4(DSP):c.3303C>T (p.Tyr1101=) rs372440854
NM_004415.4(DSP):c.3696C>A (p.Ser1232=) rs141120358
NM_004415.4(DSP):c.3923G>A (p.Arg1308Gln) rs184154918
NM_004415.4(DSP):c.422+275G>A
NM_004415.4(DSP):c.423-16_423-15insC rs113028223
NM_004415.4(DSP):c.4609C>T (p.Arg1537Cys) rs28763967
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.6351T>C (p.Asp2117=) rs148743859
NM_004415.4(DSP):c.6678T>A (p.Gly2226=) rs149070106
NM_004415.4(DSP):c.726+219T>G
NM_004415.4(DSP):c.727-206C>T
NM_004415.4(DSP):c.727-213G>A
NM_004415.4(DSP):c.7734C>T (p.Ser2578=) rs28763970
NM_004415.4(DSP):c.777+104G>A
NM_004415.4(DSP):c.777+120C>G
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.8605A>G (p.Ile2869Val) rs28763971
NM_004415.4(DSP):c.939+132G>A
NM_004415.4(DSP):c.939+195G>A
NM_004415.4(DSP):c.939+299C>T
NM_004415.4(DSP):c.940-195T>C
NM_004415.4(DSP):c.940-224T>C

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