List of variants in gene combination MUTYH, TOE1 reported as likely benign for Hereditary cancer-predisposing syndrome

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: 21

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_025077.4(TOE1):c.52+77G>A	rs3219466	0.02177
NM_025077.4(TOE1):c.-41A>G	rs1211077933	0.00005
NM_001128425.2(MUTYH):c.12C>A (p.Leu4=)	rs876659717
NM_001128425.2(MUTYH):c.12C>T (p.Leu4=)	rs876659717
NM_001128425.2(MUTYH):c.22C>T (p.Leu8=)	rs753502884
NM_001128425.2(MUTYH):c.24G>C (p.Leu8=)	rs1570591790
NM_001128425.2(MUTYH):c.28C>A (p.Arg10Ser)	rs1570591700
NM_001128425.2(MUTYH):c.31C>T (p.Leu11=)	rs878854188
NM_001128425.2(MUTYH):c.33G>A (p.Leu11=)
NM_001128425.2(MUTYH):c.9G>A (p.Pro3=)	rs958040221
NM_001128425.2(MUTYH):c.9G>C (p.Pro3=)	rs958040221
NM_001128425.2(MUTYH):c.9G>T (p.Pro3=)	rs958040221
NM_025077.4(TOE1):c.-43C>A	rs766584437
NM_025077.4(TOE1):c.-43C>T	rs766584437
NM_025077.4(TOE1):c.-44T>G	rs201746729
NM_025077.4(TOE1):c.-45G>C	rs2275602
NM_025077.4(TOE1):c.-52A>G	rs1553136902
NM_025077.4(TOE1):c.-54G>A	rs540793556
NM_025077.4(TOE1):c.-54G>C	rs540793556
NM_025077.4(TOE1):c.-54G>T	rs540793556
NM_025077.4(TOE1):c.9C>T (p.Ala3=)

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.