ClinVar Miner

List of variants in gene SPRED1 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 15q14(chr15:38570091-38647695)x3
NM_152594.3(SPRED1):c.*1724A>C rs1554527
NM_152594.3(SPRED1):c.*248T>C rs16966842
NM_152594.3(SPRED1):c.*256C>T rs145373657
NM_152594.3(SPRED1):c.*2742G>T
NM_152594.3(SPRED1):c.*2831G>A rs35490364
NM_152594.3(SPRED1):c.*3521A>G rs11634702
NM_152594.3(SPRED1):c.*3698T>G rs76527876
NM_152594.3(SPRED1):c.*3830G>A rs8039150
NM_152594.3(SPRED1):c.*3946G>A rs8039337
NM_152594.3(SPRED1):c.*3996G>A rs72725364
NM_152594.3(SPRED1):c.*427A>T rs185290497
NM_152594.3(SPRED1):c.*4662T>A rs10852019
NM_152594.3(SPRED1):c.*4932A>G rs16966843
NM_152594.3(SPRED1):c.*5110C>T rs8026118
NM_152594.3(SPRED1):c.*5398G>T
NM_152594.3(SPRED1):c.-244T>C rs138385793
NM_152594.3(SPRED1):c.-93C>T rs192699510
NM_152594.3(SPRED1):c.1044T>C (p.Val348=) rs3751526
NM_152594.3(SPRED1):c.124G>A (p.Val42Ile) rs147204964
NM_152594.3(SPRED1):c.207+15A>G rs377288061
NM_152594.3(SPRED1):c.208-18G>A rs398122371
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val) rs200157475
NM_152594.3(SPRED1):c.291G>A (p.Lys97=) rs7182445
NM_152594.3(SPRED1):c.32+20C>T
NM_152594.3(SPRED1):c.32+307A>C rs3938236
NM_152594.3(SPRED1):c.33-274A>G rs10220731
NM_152594.3(SPRED1):c.376+279_376+291del rs3841233
NM_152594.3(SPRED1):c.377-149G>A rs1879939
NM_152594.3(SPRED1):c.377-319T>C rs1916153
NM_152594.3(SPRED1):c.423+103C>T rs1879938
NM_152594.3(SPRED1):c.423+105C>G rs1879937
NM_152594.3(SPRED1):c.423+272A>G rs8036371
NM_152594.3(SPRED1):c.424-18G>A rs7179118
NM_152594.3(SPRED1):c.424-8= rs7180446
NM_152594.3(SPRED1):c.424-8C>A rs7180446
NM_152594.3(SPRED1):c.424-98= rs7163339
NM_152594.3(SPRED1):c.424-98T>C rs7163339
NM_152594.3(SPRED1):c.446G>A (p.Ser149Asn) rs373384814
NM_152594.3(SPRED1):c.582+52A>G rs7181472
NM_152594.3(SPRED1):c.583-7A>G rs115970207
NM_152594.3(SPRED1):c.675C>T (p.Ser225=) rs144764225
NM_152594.3(SPRED1):c.684+167A>G rs10083640
NM_152594.3(SPRED1):c.685-184C>T rs12914722
NM_152594.3(SPRED1):c.685-206G>A rs12913526
NM_152594.3(SPRED1):c.685-244G>C rs12913505
NM_152594.3(SPRED1):c.879G>A (p.Leu293=) rs535687467
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala) rs114636635
NM_152594.3(SPRED1):c.939G>A (p.Thr313=) rs140644874
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.