ClinVar Miner

List of variants in gene ARID1B reported by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001374828.1(ARID1B):c.2629C>T (p.Pro877Ser) rs114201726 0.00727
NM_001374828.1(ARID1B):c.3106G>A (p.Gly1036Ser) rs34786733 0.00590
NM_001374828.1(ARID1B):c.985G>A (p.Gly329Ser) rs375160616 0.00475
NM_001374828.1(ARID1B):c.3235+6C>T rs148976215 0.00384
NM_001374828.1(ARID1B):c.1791+19G>C rs374013482 0.00249
NM_001374828.1(ARID1B):c.3714+11G>A rs368322992 0.00159
NM_001374828.1(ARID1B):c.4603T>G (p.Ser1535Ala) rs145516400 0.00016
NM_001374828.1(ARID1B):c.6641T>C (p.Ile2214Thr) rs878852997 0.00004
NM_001374828.1(ARID1B):c.5914C>A (p.Pro1972Thr) rs779490460 0.00002
NM_001374828.1(ARID1B):c.1170CGG[4] (p.Gly399_Gly402del) rs587779747
NM_001374828.1(ARID1B):c.1170CGG[9] (p.Gly402dup) rs587779747
NM_001374828.1(ARID1B):c.1211GAG[9] (p.Gly411dup) rs747790383
NM_001374828.1(ARID1B):c.1268C>T (p.Ala423Val) rs878853084
NM_001374828.1(ARID1B):c.1292CAG[4] (p.Ala433dup) rs797045267
NM_001374828.1(ARID1B):c.1303GGC[7] (p.Gly440dup) rs797045268
NM_001374828.1(ARID1B):c.6072dup (p.Lys2025Ter) rs886041878

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.