ClinVar Miner

List of variants in gene ATRX reported as likely pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_000489.5(ATRX):c.2102G>A (p.Arg701His) rs797044563
NM_000489.5(ATRX):c.371-2A>G rs1557148369
NM_000489.5(ATRX):c.4509A>T (p.Arg1503Ser) rs1057517997
NM_000489.5(ATRX):c.5072A>C (p.Gln1691Pro) rs1569533321
NM_000489.5(ATRX):c.6254G>A (p.Arg2085His) rs1057517948
NM_000489.5(ATRX):c.6532C>T (p.Arg2178Trp) rs1057517707
NM_000489.5(ATRX):c.668G>A (p.Cys223Tyr) rs1557142844
NM_000489.5(ATRX):c.7147G>C (p.Asp2383His) rs1057518225
NM_000489.5(ATRX):c.7219C>T (p.Arg2407Ter) rs1557034957
NM_000489.5(ATRX):c.729C>G (p.Cys243Trp) rs1057524153
NM_000489.5(ATRX):c.7364_7365AT[1] (p.Met2456fs) rs797044723

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.