ClinVar Miner

List of variants studied for T-cell acute lymphoblastic leukemia

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000051.4(ATM):c.7271T>G (p.Val2424Gly) rs28904921 0.00006
NM_022552.5(DNMT3A):c.1204C>T (p.Gln402Ter) rs796065342 0.00001
NM_000051.4(ATM):c.5044G>C (p.Asp1682His) rs121434217
NM_000051.4(ATM):c.5309C>G (p.Ser1770Ter) rs121434223
NM_000051.4(ATM):c.7638_7646del (p.Arg2547_Ser2549del) rs587776547
NM_000760.4(CSF3R):c.1853C>T (p.Thr618Ile) rs796065343
NM_002834.5(PTPN11):c.854T>C (p.Phe285Ser) rs121918463
NM_003921.5(BCL10):c.136dup (p.Ile46fs) rs387906351
NM_017617.5(NOTCH1):c.4775T>G (p.Phe1592Cys) rs796065341
NM_138761.4(BAX):c.115_121del (p.Gly39fs) rs398122840
NM_138761.4(BAX):c.199G>A (p.Gly67Arg) rs398122513
Single allele

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.