List of variants studied for bone cancer by 3billion

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004972.4(JAK2):c.1849G>T (p.Val617Phe)	rs77375493	0.00037
NM_001754.5(RUNX1):c.154A>G (p.Met52Val)	rs2517487761
NM_004119.3(FLT3):c.2533A>G (p.Arg845Gly)	rs2137622655
NM_004972.4(JAK2):c.2861T>G (p.Leu954Arg)
NM_005157.6(ABL1):c.944C>T (p.Thr315Ile)	rs121913459

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.