ClinVar Miner

List of variants reported as other for Neuroblastoma

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000142.5(FGFR3):c.991T>C (p.Phe331Leu) rs1246952737 0.00001
NM_000059.4(BRCA2):c.1075G>A (p.Glu359Lys) rs1555281730
NM_000245.4(MET):c.985C>A (p.Leu329Ile) rs1554378983
NM_000548.5(TSC2):c.3284+1G>T rs45517289
NM_001015877.2(PHF6):c.119C>A (p.Ala40Glu) rs1556013242
NM_003010.4(MAP2K4):c.538C>G (p.Leu180Val) rs1555550018
NM_006180.6(NTRK2):c.970T>A (p.Leu324Met) rs201362502
NM_022768.5(RBM15):c.1912C>A (p.Gln638Lys) rs1553224979
NM_145185.4(MAP2K7):c.752T>C (p.Leu251Pro) rs1555701191

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.