ClinVar Miner

List of variants reported as likely pathogenic for Metastatic pancreatic neuroendocrine tumours

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.3504G>T (p.Met1168Ile) rs1555283267
NM_000489.6(ATRX):c.1558G>T (p.Val520Phe) rs1287383551
NM_000546.6(TP53):c.818G>T (p.Arg273Leu) rs28934576
NM_001141969.2(DAXX):c.1178del (p.Lys393fs) rs1359674497
NM_001141969.2(DAXX):c.329_330del (p.Leu109_Ser110insTer) rs1554283140
NM_001141969.2(DAXX):c.801_824del (p.Arg269_Asn276del) rs1554282803
NM_001141969.2(DAXX):c.850C>T (p.Pro284Ser) rs1554282793
NM_001370259.2(MEN1):c.1579C>T (p.Arg527Ter) rs104894261
NM_001370259.2(MEN1):c.245_259del (p.Asp82_Ile86del) rs1555166508
NM_001370259.2(MEN1):c.783+1G>A rs794728652
NM_001370259.2(MEN1):c.981_1006del (p.Tyr327_Glu336delinsTer) rs1555165008
NM_004958.4(MTOR):c.6625C>G (p.Leu2209Val) rs774204282

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.