ClinVar Miner

List of variants in gene SPRED1 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP
NM_152594.3(SPRED1):c.1005C>T (p.Cys335=) rs768937237
NM_152594.3(SPRED1):c.1146C>T (p.Asp382=) rs1286583801
NM_152594.3(SPRED1):c.1176G>A (p.Ser392=) rs755223172
NM_152594.3(SPRED1):c.1191C>T (p.Asp397=) rs749745659
NM_152594.3(SPRED1):c.1215A>G (p.Leu405=) rs1595764001
NM_152594.3(SPRED1):c.1225_1226delinsTT (p.Ala409Phe) rs1566877075
NM_152594.3(SPRED1):c.174T>C (p.Phe58=) rs1595733589
NM_152594.3(SPRED1):c.207+15A>G rs377288061
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val) rs200157475
NM_152594.3(SPRED1):c.321T>C (p.Ala107=) rs770197803
NM_152594.3(SPRED1):c.33-7A>G rs760850290
NM_152594.3(SPRED1):c.377-10A>G rs376134678
NM_152594.3(SPRED1):c.384C>T (p.Pro128=) rs761058615
NM_152594.3(SPRED1):c.51G>A (p.Val17=) rs864622421
NM_152594.3(SPRED1):c.531C>T (p.Pro177=) rs1595756882
NM_152594.3(SPRED1):c.594T>C (p.Gly198=) rs756643495
NM_152594.3(SPRED1):c.636A>C (p.Val212=) rs1057523137
NM_152594.3(SPRED1):c.669A>G (p.Leu223=) rs774530752
NM_152594.3(SPRED1):c.687C>T (p.Val229=) rs376226762
NM_152594.3(SPRED1):c.879G>A (p.Leu293=) rs535687467
NM_152594.3(SPRED1):c.933T>C (p.Phe311=) rs1057522873
NM_152594.3(SPRED1):c.939G>A (p.Thr313=) rs140644874
NM_152594.3(SPRED1):c.948C>G (p.Ser316=) rs1595763720
NM_152594.3(SPRED1):c.963G>A (p.Lys321=) rs369711772

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.