ClinVar Miner

List of variants in gene PAN3 reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_175854.8(PAN3):c.1478G>A (p.Arg493Gln) rs140429993 0.00019
NM_175854.8(PAN3):c.521G>A (p.Ser174Asn) rs145640790 0.00007
NM_175854.8(PAN3):c.2608C>T (p.Arg870Cys) rs752562748 0.00006
NM_175854.8(PAN3):c.2217G>A (p.Met739Ile) rs537694851 0.00004
NM_175854.8(PAN3):c.712A>T (p.Met238Leu) rs750690809 0.00004
NM_175854.8(PAN3):c.1258A>G (p.Asn420Asp) rs377198462 0.00003
NM_175854.8(PAN3):c.836C>G (p.Thr279Arg) rs377685978 0.00003
NM_175854.8(PAN3):c.463A>G (p.Thr155Ala) rs151232852 0.00002
NM_175854.8(PAN3):c.1144C>G (p.Pro382Ala) rs776461410 0.00001
NM_175854.8(PAN3):c.1460C>T (p.Pro487Leu) rs1258314786 0.00001
NM_175854.8(PAN3):c.1531A>G (p.Asn511Asp) rs766481765 0.00001
NM_175854.8(PAN3):c.1793G>C (p.Gly598Ala) rs1306827589 0.00001
NM_175854.8(PAN3):c.1807C>G (p.Pro603Ala) rs201794415 0.00001
NM_175854.8(PAN3):c.1907T>C (p.Leu636Ser) rs1003722207 0.00001
NM_175854.8(PAN3):c.1942A>G (p.Ile648Val) rs778986227 0.00001
NM_175854.8(PAN3):c.2272G>A (p.Asp758Asn) rs752637077 0.00001
NM_175854.8(PAN3):c.2297T>C (p.Val766Ala) rs1187877186 0.00001
NM_175854.8(PAN3):c.839A>G (p.Glu280Gly) rs1232692926 0.00001
NM_175854.8(PAN3):c.1080A>T (p.Arg360Ser)
NM_175854.8(PAN3):c.1121G>C (p.Ser374Thr) rs768803539
NM_175854.8(PAN3):c.1163C>T (p.Ser388Phe)
NM_175854.8(PAN3):c.1187A>G (p.Glu396Gly) rs2501896904
NM_175854.8(PAN3):c.121G>T (p.Ala41Ser)
NM_175854.8(PAN3):c.122C>T (p.Ala41Val)
NM_175854.8(PAN3):c.124G>T (p.Val42Leu) rs985989145
NM_175854.8(PAN3):c.1267A>G (p.Ile423Val)
NM_175854.8(PAN3):c.127G>A (p.Gly43Arg) rs2500742637
NM_175854.8(PAN3):c.1280C>A (p.Thr427Asn)
NM_175854.8(PAN3):c.1288C>A (p.His430Asn)
NM_175854.8(PAN3):c.1377A>G (p.Ile459Met)
NM_175854.8(PAN3):c.1510A>G (p.Thr504Ala) rs773602437
NM_175854.8(PAN3):c.1760A>C (p.Asn587Thr) rs2501999199
NM_175854.8(PAN3):c.1788G>C (p.Lys596Asn) rs773169905
NM_175854.8(PAN3):c.1788G>T (p.Lys596Asn) rs773169905
NM_175854.8(PAN3):c.23C>T (p.Pro8Leu)
NM_175854.8(PAN3):c.2497A>G (p.Ser833Gly)
NM_175854.8(PAN3):c.482A>C (p.Tyr161Ser)
NM_175854.8(PAN3):c.490A>G (p.Thr164Ala) rs1263784721
NM_175854.8(PAN3):c.575C>T (p.Ser192Phe) rs1222937477
NM_175854.8(PAN3):c.616C>T (p.His206Tyr)
NM_175854.8(PAN3):c.788G>C (p.Arg263Thr) rs1878173523
NM_175854.8(PAN3):c.808A>G (p.Ile270Val)
NM_175854.8(PAN3):c.829A>G (p.Arg277Gly) rs757082745
NM_175854.8(PAN3):c.898A>G (p.Thr300Ala)

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.