List of variants in gene DSP reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 50

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HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.2596C>T (p.Arg866Cys)	rs142429411	0.00214
NM_004415.4(DSP):c.2773C>T (p.Arg925Trp)	rs145933612	0.00143
NM_004415.4(DSP):c.2683T>C (p.Tyr895His)	rs375891215	0.00043
NM_004415.4(DSP):c.5178C>A (p.Asn1726Lys)	rs147415451	0.00033
NM_004415.4(DSP):c.8467C>G (p.Pro2823Ala)	rs142717240	0.00020
NM_004415.4(DSP):c.269A>G (p.Gln90Arg)	rs188516326	0.00018
NM_004415.4(DSP):c.2121C>T (p.Asn707=)	rs368590198	0.00017
NM_004415.4(DSP):c.4775A>G (p.Lys1592Arg)	rs200421954	0.00016
NM_004415.4(DSP):c.1575-15C>G	rs369184165	0.00013
NM_004415.4(DSP):c.2037A>G (p.Ile679Met)	rs151049942	0.00012
NM_004415.4(DSP):c.1483G>A (p.Val495Met)	rs372014020	0.00011
NM_004415.4(DSP):c.6799A>T (p.Thr2267Ser)	rs181378432	0.00011
NM_004415.4(DSP):c.3616T>A (p.Leu1206Ile)	rs151115778	0.00010
NM_004415.4(DSP):c.987G>A (p.Leu329=)	rs564435126	0.00010
NM_004415.4(DSP):c.4175G>A (p.Arg1392Gln)	rs201736018	0.00009
NM_004415.4(DSP):c.5523A>C (p.Ser1841=)	rs730882116	0.00009
NM_004415.4(DSP):c.1044+12G>A	rs775969969	0.00007
NM_004415.4(DSP):c.7563T>C (p.Asp2521=)	rs984412074	0.00007
NM_004415.4(DSP):c.1155G>A (p.Ala385=)	rs140488069	0.00006
NM_004415.4(DSP):c.2630+19G>A	rs139830549	0.00006
NM_004415.4(DSP):c.2247A>G (p.Leu749=)	rs28763963	0.00005
NM_004415.4(DSP):c.4401A>G (p.Gln1467=)	rs199818953	0.00005
NM_004415.4(DSP):c.5555G>A (p.Arg1852His)	rs193922669	0.00005
NM_004415.4(DSP):c.2360A>G (p.Tyr787Cys)	rs778350289	0.00004
NM_004415.4(DSP):c.4741A>G (p.Lys1581Glu)	rs186842903	0.00003
NM_004415.4(DSP):c.2046C>T (p.Cys682=)	rs771674559	0.00002
NM_004415.4(DSP):c.8394T>A (p.Thr2798=)	rs775346694	0.00002
NM_004415.4(DSP):c.1482C>T (p.Tyr494=)	rs772925425	0.00001
NM_004415.4(DSP):c.1821A>G (p.Lys607=)	rs768675424	0.00001
NM_004415.4(DSP):c.4566G>A (p.Thr1522=)	rs1159243386	0.00001
NM_004415.4(DSP):c.5202G>C (p.Leu1734=)	rs755220841	0.00001
NM_004415.4(DSP):c.5631T>C (p.Ala1877=)	rs1231651139	0.00001
NM_004415.4(DSP):c.5880C>T (p.Thr1960=)	rs375883982	0.00001
NM_004415.4(DSP):c.7413A>G (p.Pro2471=)	rs772161814	0.00001
NM_004415.4(DSP):c.1161T>A (p.Ser387=)	rs1758909456
NM_004415.4(DSP):c.157T>G (p.Ser53Ala)	rs397516918
NM_004415.4(DSP):c.319T>C (p.Leu107=)
NM_004415.4(DSP):c.3462T>A (p.Gly1154=)	rs1554108086
NM_004415.4(DSP):c.3956C>G (p.Thr1319Ser)	rs138599871
NM_004415.4(DSP):c.4521A>G (p.Leu1507=)	rs1060500611
NM_004415.4(DSP):c.5116C>T (p.Leu1706=)	rs1759432452
NM_004415.4(DSP):c.6072T>C (p.Ser2024=)
NM_004415.4(DSP):c.6153C>G (p.Ala2051=)	rs193922670
NM_004415.4(DSP):c.6558G>A (p.Leu2186=)	rs1759540433
NM_004415.4(DSP):c.6993T>C (p.Ser2331=)	rs767282172
NM_004415.4(DSP):c.7893C>T (p.Ile2631=)	rs778552693
NM_004415.4(DSP):c.8111AGA[2] (p.Lys2706del)	rs397516962
NM_004415.4(DSP):c.8320C>T (p.Leu2774=)	rs397516964
NM_004415.4(DSP):c.8454C>T (p.Asn2818=)
NM_004415.4(DSP):c.8490C>A (p.Arg2830=)	rs1221382084

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