ClinVar Miner

List of variants in gene INPP5E reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 57
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_019892.6(INPP5E):c.623C>T (p.Thr208Ile) rs143107549 0.00177
NM_019892.6(INPP5E):c.21T>C (p.Asn7=) rs571588033 0.00135
NM_019892.6(INPP5E):c.1875G>A (p.Glu625=) rs148539728 0.00128
NM_019892.6(INPP5E):c.1803-20C>T rs190316580 0.00057
NM_019892.6(INPP5E):c.1191C>T (p.Ile397=) rs558778286 0.00029
NM_019892.6(INPP5E):c.183G>A (p.Glu61=) rs570404672 0.00027
NM_019892.6(INPP5E):c.1549+40G>A rs11146013 0.00022
NM_019892.6(INPP5E):c.1387+8C>T rs374620221 0.00013
NM_019892.6(INPP5E):c.1176G>A (p.Thr392=) rs528176529 0.00009
NM_019892.6(INPP5E):c.588C>T (p.Ala196=) rs368034918 0.00008
NM_019892.6(INPP5E):c.1387+9G>A rs202236947 0.00007
NM_019892.6(INPP5E):c.1410T>C (p.Asp470=) rs138552060 0.00007
NM_019892.6(INPP5E):c.1104C>T (p.His368=) rs148592275 0.00006
NM_019892.6(INPP5E):c.976G>A (p.Glu326Lys) rs200794870 0.00006
NM_019892.6(INPP5E):c.1035-9C>T rs750624613 0.00005
NM_019892.6(INPP5E):c.-175C>T rs868202242 0.00004
NM_019892.6(INPP5E):c.1280-10G>A rs780428016 0.00004
NM_019892.6(INPP5E):c.1388-5C>T rs187956407 0.00004
NM_019892.6(INPP5E):c.1389G>A (p.Ala463=) rs779735920 0.00004
NM_019892.6(INPP5E):c.1758T>C (p.Pro586=) rs1222127887 0.00004
NM_019892.6(INPP5E):c.1881G>A (p.Gln627=) rs144720715 0.00004
NM_019892.6(INPP5E):c.516G>T (p.Pro172=) rs372551521 0.00004
NM_019892.6(INPP5E):c.1374T>C (p.Tyr458=) rs886038652 0.00003
NM_019892.6(INPP5E):c.843C>T (p.Ser281=) rs375981295 0.00003
NM_019892.6(INPP5E):c.1224C>T (p.Gly408=) rs769914491 0.00002
NM_019892.6(INPP5E):c.363C>T (p.Pro121=) rs762231724 0.00002
NM_019892.6(INPP5E):c.853T>C (p.Leu285=) rs763694461 0.00002
NM_019892.6(INPP5E):c.1452C>T (p.Gly484=) rs371729050 0.00001
NM_019892.6(INPP5E):c.1551G>T (p.Gly517=) rs201644680 0.00001
NM_019892.6(INPP5E):c.1746C>T (p.Ser582=) rs888901624 0.00001
NM_019892.6(INPP5E):c.201A>G (p.Ala67=) rs754529136 0.00001
NM_019892.6(INPP5E):c.687G>C (p.Arg229=) rs958712451 0.00001
NM_019892.6(INPP5E):c.*5T>G
NM_019892.6(INPP5E):c.-28C>T
NM_019892.6(INPP5E):c.1034+8G>A rs201272028
NM_019892.6(INPP5E):c.1035-8_1035-6del rs1226334444
NM_019892.6(INPP5E):c.1065G>A (p.Thr355=) rs374089192
NM_019892.6(INPP5E):c.1065G>C (p.Thr355=) rs374089192
NM_019892.6(INPP5E):c.1159+7_1159+8insGGTGGGCGTGGCTGGAGG rs71269007
NM_019892.6(INPP5E):c.1160-7C>G
NM_019892.6(INPP5E):c.120C>G (p.Pro40=)
NM_019892.6(INPP5E):c.1219T>C (p.Leu407=)
NM_019892.6(INPP5E):c.1280-11T>C rs886038651
NM_019892.6(INPP5E):c.1280-8T>A
NM_019892.6(INPP5E):c.12G>A (p.Lys4=)
NM_019892.6(INPP5E):c.1543C>A (p.Arg515=) rs13297509
NM_019892.6(INPP5E):c.1743G>C (p.Thr581=) rs368026621
NM_019892.6(INPP5E):c.1803-40_1803-7del
NM_019892.6(INPP5E):c.1897C>G (p.Gln633Glu)
NM_019892.6(INPP5E):c.210C>T (p.Ile70=) rs1444322599
NM_019892.6(INPP5E):c.255C>T (p.Ser85=) rs776746807
NM_019892.6(INPP5E):c.597G>A (p.Leu199=)
NM_019892.6(INPP5E):c.627A>G (p.Ala209=)
NM_019892.6(INPP5E):c.915C>T (p.Thr305=)
NM_019892.6(INPP5E):c.936+4_936+5dup rs2131611229
NM_019892.6(INPP5E):c.975C>G (p.Ala325=) rs143258290
NM_019892.6(INPP5E):c.975C>T (p.Ala325=) rs143258290

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.