ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 40
Download table as spreadsheet
HGVS dbSNP
NM_004415.3(DSP):c.2630+1delG rs1554107651
NM_004415.4(DSP):c.1054_1059delinsCA (p.Asp352fs) rs1064793435
NM_004415.4(DSP):c.123C>G (p.Tyr41Ter) rs1057523045
NM_004415.4(DSP):c.1266+2T>C rs1554106756
NM_004415.4(DSP):c.1513G>T (p.Val505Phe) rs794728113
NM_004415.4(DSP):c.1650G>A (p.Trp550Ter) rs397516919
NM_004415.4(DSP):c.1790C>T (p.Ser597Leu) rs606231294
NM_004415.4(DSP):c.1903+1G>C rs1554107107
NM_004415.4(DSP):c.2297+1G>A rs1057523629
NM_004415.4(DSP):c.2436+2T>C rs774514264
NM_004415.4(DSP):c.2437-1G>C rs1057517903
NM_004415.4(DSP):c.2684A>G (p.Tyr895Cys) rs367752002
NM_004415.4(DSP):c.2985G>A (p.Glu995=) rs768858918
NM_004415.4(DSP):c.2T>G (p.Met1Arg) rs748738880
NM_004415.4(DSP):c.3049_3050dup (p.Leu1017fs) rs794728157
NM_004415.4(DSP):c.3316G>T (p.Glu1106Ter) rs1131691673
NM_004415.4(DSP):c.3788_3789dup (p.Thr1264fs) rs1554108170
NM_004415.4(DSP):c.3799C>T (p.Arg1267Ter) rs121912997
NM_004415.4(DSP):c.3865C>T (p.Gln1289Ter) rs778178956
NM_004415.4(DSP):c.4026G>A (p.Trp1342Ter) rs1561698345
NM_004415.4(DSP):c.4297C>T (p.Gln1433Ter) rs1554108283
NM_004415.4(DSP):c.4822C>T (p.Gln1608Ter) rs1060500610
NM_004415.4(DSP):c.4882_4886delinsTTCT (p.Arg1628fs) rs1554108410
NM_004415.4(DSP):c.4954del (p.Glu1652fs)
NM_004415.4(DSP):c.5321_5322AG[3] (p.Glu1776fs) rs1394836623
NM_004415.4(DSP):c.5460dup (p.Val1821fs) rs1554108609
NM_004415.4(DSP):c.5680_5683del (p.Ser1894fs) rs774763657
NM_004415.4(DSP):c.5800C>T (p.Arg1934Ter) rs121912996
NM_004415.4(DSP):c.6273del (p.Ala2092fs) rs794728146
NM_004415.4(DSP):c.6393del (p.Gly2133fs) rs730880093
NM_004415.4(DSP):c.6456dup (p.Leu2153fs) rs1554108854
NM_004415.4(DSP):c.6907G>C (p.Asp2303His) rs794728131
NM_004415.4(DSP):c.6937del (p.Glu2313fs) rs794728143
NM_004415.4(DSP):c.7066A>T (p.Lys2356Ter) rs1561703331
NM_004415.4(DSP):c.7487_7488TG[2] (p.Cys2497_Glu2498delinsTer) rs754354190
NM_004415.4(DSP):c.7641C>G (p.Tyr2547Ter) rs1464253797
NM_004415.4(DSP):c.8442dup (p.Ser2815fs) rs1554109247
NM_004415.4(DSP):c.8476C>T (p.Arg2826Cys) rs139969658
NM_004415.4(DSP):c.939+1G>A rs727504443
NM_004415.4(DSP):c.942del (p.Arg315fs)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.