ClinVar Miner

List of variants in gene ARID1B reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001374828.1(ARID1B):c.980C>G (p.Pro327Arg) rs775385239 0.00018
NM_001374828.1(ARID1B):c.1712C>G (p.Pro571Arg) rs769085274 0.00004
NM_001374828.1(ARID1B):c.3266C>T (p.Pro1089Leu) rs540277176 0.00004
NM_001374828.1(ARID1B):c.4505T>C (p.Met1502Thr) rs145012943 0.00004
NM_001374828.1(ARID1B):c.4829C>T (p.Ala1610Val) rs370838091 0.00004
NM_001374828.1(ARID1B):c.4459G>A (p.Gly1487Ser) rs151115781 0.00003
NM_001374828.1(ARID1B):c.2615T>C (p.Met872Thr) rs761093701 0.00002
NM_001374828.1(ARID1B):c.3304G>A (p.Gly1102Ser) rs375023508 0.00002
NM_001374828.1(ARID1B):c.6724G>A (p.Val2242Ile) rs771871664 0.00002
NM_001374828.1(ARID1B):c.1439C>T (p.Ser480Leu) rs1235258455 0.00001
NM_001374828.1(ARID1B):c.3236-1G>A rs752642190 0.00001
NM_001374828.1(ARID1B):c.961G>T (p.Ala321Ser) rs1268089519 0.00001
NC_000006.12:g.157174010_157174024del rs2128303771
NM_001374828.1(ARID1B):c.1051TCCGCC[3] (p.Ala354_Ala355insSerAla)
NM_001374828.1(ARID1B):c.1175G>A (p.Gly392Asp)
NM_001374828.1(ARID1B):c.1205G>A (p.Gly402Asp)
NM_001374828.1(ARID1B):c.1312G>A (p.Gly438Ser)
NM_001374828.1(ARID1B):c.1433C>T (p.Ala478Val) rs1778972122
NM_001374828.1(ARID1B):c.1652A>G (p.Gln551Arg) rs1779010461
NM_001374828.1(ARID1B):c.1669G>C (p.Gly557Arg)
NM_001374828.1(ARID1B):c.1700C>T (p.Ala567Val)
NM_001374828.1(ARID1B):c.2054G>C (p.Ser685Thr)
NM_001374828.1(ARID1B):c.2174C>T (p.Pro725Leu)
NM_001374828.1(ARID1B):c.2582-1G>T rs1788656400
NM_001374828.1(ARID1B):c.2981C>G (p.Ser994Cys) rs1789987223
NM_001374828.1(ARID1B):c.3164A>G (p.Asn1055Ser)
NM_001374828.1(ARID1B):c.3316G>A (p.Gly1106Ser) rs1583451251
NM_001374828.1(ARID1B):c.3830G>A (p.Cys1277Tyr)
NM_001374828.1(ARID1B):c.3985G>A (p.Val1329Ile)
NM_001374828.1(ARID1B):c.4245C>G (p.Ser1415Arg) rs1453138221
NM_001374828.1(ARID1B):c.4490G>A (p.Arg1497His)
NM_001374828.1(ARID1B):c.4835C>T (p.Pro1612Leu)
NM_001374828.1(ARID1B):c.5503G>C (p.Asp1835His)
NM_001374828.1(ARID1B):c.5659G>T (p.Ala1887Ser)
NM_001374828.1(ARID1B):c.5875A>G (p.Ser1959Gly)
NM_001374828.1(ARID1B):c.6150C>G (p.Asp2050Glu) rs779936373
NM_001374828.1(ARID1B):c.6913A>G (p.Met2305Val) rs1181252259

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.