List of variants in gene KMT2A reported as likely benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001197104.2(KMT2A):c.6572G>A (p.Arg2191Gln)	rs141727765	0.00109
NM_001197104.2(KMT2A):c.2965C>T (p.Leu989Phe)	rs139989306	0.00101
NM_001197104.2(KMT2A):c.6009C>T (p.Asp2003=)	rs77421119	0.00086
NM_001197104.2(KMT2A):c.10715T>G (p.Ile3572Ser)	rs147014136	0.00051
NM_001197104.2(KMT2A):c.1810A>G (p.Met604Val)	rs150328852	0.00046
NM_001197104.2(KMT2A):c.10113G>A (p.Arg3371=)	rs369292004	0.00013
NM_001197104.2(KMT2A):c.9769T>C (p.Leu3257=)	rs138046203	0.00011
NM_001197104.2(KMT2A):c.10690C>T (p.Arg3564Trp)	rs555310772	0.00003
NM_001197104.2(KMT2A):c.10178T>C (p.Leu3393Pro)	rs1555048205
NM_001197104.2(KMT2A):c.10580G>A (p.Arg3527Gln)	rs147844226
NM_001197104.2(KMT2A):c.2544G>C (p.Gly848=)
NM_001197104.2(KMT2A):c.9478T>C (p.Ser3160Pro)	rs1555047715

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.