ClinVar Miner

List of variants in gene SPRED1 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 92
Download table as spreadsheet
HGVS dbSNP
NM_152594.3(SPRED1):c.*1040G>A rs115568221
NM_152594.3(SPRED1):c.*1659_*1662del rs57589132
NM_152594.3(SPRED1):c.*2018T>G
NM_152594.3(SPRED1):c.*2247A>G
NM_152594.3(SPRED1):c.*2570T>C rs111997668
NM_152594.3(SPRED1):c.*2611C>T
NM_152594.3(SPRED1):c.*2885G>A rs79309779
NM_152594.3(SPRED1):c.*3057A>G rs72725362
NM_152594.3(SPRED1):c.*3561G>A
NM_152594.3(SPRED1):c.*3591C>T rs147489619
NM_152594.3(SPRED1):c.*3623G>T rs148525432
NM_152594.3(SPRED1):c.*4372A>G
NM_152594.3(SPRED1):c.*4697G>A
NM_152594.3(SPRED1):c.*5090dup rs141174183
NM_152594.3(SPRED1):c.*5202C>T rs541213700
NM_152594.3(SPRED1):c.*581T>C
NM_152594.3(SPRED1):c.*633A>G
NM_152594.3(SPRED1):c.-156del rs531519324
NM_152594.3(SPRED1):c.-191C>T rs556907443
NM_152594.3(SPRED1):c.-294_-293CT[2] rs1048605006
NM_152594.3(SPRED1):c.1005C>T (p.Cys335=) rs768937237
NM_152594.3(SPRED1):c.1008A>G (p.Val336=) rs1555392775
NM_152594.3(SPRED1):c.1080A>G (p.Lys360=)
NM_152594.3(SPRED1):c.1110C>G (p.Leu370=) rs876657584
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.1192G>A (p.Asp398Asn) rs771480941
NM_152594.3(SPRED1):c.1194C>T (p.Asp398=)
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.123C>T (p.Ser41=)
NM_152594.3(SPRED1):c.124G>A (p.Val42Ile) rs147204964
NM_152594.3(SPRED1):c.1260C>T (p.Tyr420=)
NM_152594.3(SPRED1):c.1278C>T (p.Cys426=)
NM_152594.3(SPRED1):c.1285T>C (p.Cys429Arg)
NM_152594.3(SPRED1):c.15G>C (p.Thr5=)
NM_152594.3(SPRED1):c.174T>C (p.Phe58=) rs1595733589
NM_152594.3(SPRED1):c.177T>C (p.Phe59=) rs397517871
NM_152594.3(SPRED1):c.207+15A>G rs377288061
NM_152594.3(SPRED1):c.207+37A>G rs2272105
NM_152594.3(SPRED1):c.208-10C>G
NM_152594.3(SPRED1):c.208-6T>C rs1241478218
NM_152594.3(SPRED1):c.211G>A (p.Val71Ile)
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val) rs200157475
NM_152594.3(SPRED1):c.279G>A (p.Lys93=)
NM_152594.3(SPRED1):c.27C>T (p.Asp9=) rs727504717
NM_152594.3(SPRED1):c.282T>G (p.Ile94Met)
NM_152594.3(SPRED1):c.290_291delinsGA (p.Lys97Arg) rs1555391042
NM_152594.3(SPRED1):c.306G>A (p.Thr102=) rs372791883
NM_152594.3(SPRED1):c.30C>A (p.Asn10Lys) rs201692618
NM_152594.3(SPRED1):c.321T>C (p.Ala107=) rs770197803
NM_152594.3(SPRED1):c.33-11A>G rs775671940
NM_152594.3(SPRED1):c.33-7A>G rs760850290
NM_152594.3(SPRED1):c.348C>T (p.Ile116=)
NM_152594.3(SPRED1):c.376+10C>A
NM_152594.3(SPRED1):c.376+3A>T rs775985211
NM_152594.3(SPRED1):c.377-10A>G rs376134678
NM_152594.3(SPRED1):c.384C>T (p.Pro128=) rs761058615
NM_152594.3(SPRED1):c.424-5A>G rs752656697
NM_152594.3(SPRED1):c.510C>T (p.Ser170=)
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.535G>A (p.Glu179Lys)
NM_152594.3(SPRED1):c.552A>G (p.Arg184=)
NM_152594.3(SPRED1):c.583-7A>G rs115970207
NM_152594.3(SPRED1):c.587C>T (p.Thr196Ile) rs147474792
NM_152594.3(SPRED1):c.594T>C (p.Gly198=) rs756643495
NM_152594.3(SPRED1):c.634G>A (p.Val212Ile) rs769630742
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.675C>T (p.Ser225=) rs144764225
NM_152594.3(SPRED1):c.684+10G>A rs1555392611
NM_152594.3(SPRED1):c.685-8T>C rs760690837
NM_152594.3(SPRED1):c.687C>A (p.Val229=)
NM_152594.3(SPRED1):c.687C>T (p.Val229=) rs376226762
NM_152594.3(SPRED1):c.702C>G (p.Ile234Met) rs138553244
NM_152594.3(SPRED1):c.703A>C (p.Arg235=) rs1177047281
NM_152594.3(SPRED1):c.879G>A (p.Leu293=) rs535687467
NM_152594.3(SPRED1):c.886T>C (p.Cys296Arg) rs554327738
NM_152594.3(SPRED1):c.915C>G (p.Pro305=)
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala) rs114636635
NM_152594.3(SPRED1):c.933T>C (p.Phe311=) rs1057522873
NM_152594.3(SPRED1):c.938C>T (p.Thr313Met) rs766814966
NM_152594.3(SPRED1):c.939G>A (p.Thr313=) rs140644874
NM_152594.3(SPRED1):c.939G>T (p.Thr313=)
NM_152594.3(SPRED1):c.944C>T (p.Pro315Leu) rs115440602
NM_152594.3(SPRED1):c.948C>G (p.Ser316=) rs1595763720
NM_152594.3(SPRED1):c.963G>A (p.Lys321=) rs369711772
NM_152594.3(SPRED1):c.990T>G (p.Gly330=)
NM_152594.3(SPRED1):c.997T>G (p.Ser333Ala)
NM_152594.3(SPRED1):c.9G>A (p.Glu3=)

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.