ClinVar Miner

Submissions for variant NM_001904.4(CTNNB1):c.101G>A (p.Gly34Glu)

dbSNP: rs28931589
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 11
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000019149 SCV000039437 pathogenic Pilomatrixoma 1999-04-01 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000422250 SCV000505412 likely pathogenic Squamous cell carcinoma of the head and neck 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000432939 SCV000505413 likely pathogenic Adrenal cortex carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000439589 SCV000505414 likely pathogenic Lung adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000423249 SCV000505415 likely pathogenic Gastric adenocarcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000433938 SCV000505416 likely pathogenic Malignant neoplasm of body of uterus 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443851 SCV000505417 likely pathogenic Hepatocellular carcinoma 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000426491 SCV000505418 likely pathogenic Neoplasm of ovary 2015-07-14 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000434538 SCV000505419 likely pathogenic Malignant melanoma of skin 2016-05-31 no assertion criteria provided literature only
Database of Curated Mutations (DoCM) RCV000443977 SCV000505420 likely pathogenic Medulloblastoma 2016-05-31 no assertion criteria provided literature only
Donald Williams Parsons Laboratory, Baylor College of Medicine RCV000443977 SCV000599908 other Medulloblastoma 2016-05-01 no assertion criteria provided clinical testing

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.