ClinVar Miner

List of variants in gene ARID1B reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 111
Download table as spreadsheet
HGVS dbSNP
NM_001374828.1(ARID1B):c.1360C>G (p.Pro454Ala)
NM_001374828.1(ARID1B):c.2736A>G (p.Pro912=)
NM_001374828.1(ARID1B):c.3245G>T (p.Gly1082Val)
NM_001374828.1(ARID1B):c.5442G>C (p.Leu1814=)
NM_017519.2(ARID1B):c.1016_1021dup (p.Val339_Ala340dup) rs759630370
NM_017519.2(ARID1B):c.1017_1019GGC[6] (p.Ala349_Ala350dup) rs765410747
NM_017519.2(ARID1B):c.1019C>T (p.Ala340Val) rs878853084
NM_017519.2(ARID1B):c.1029_1040del (p.Ala347_Ala350del) rs763063242
NM_017519.2(ARID1B):c.1029_1043del (p.Ala346_Ala350del) rs775733700
NM_017519.2(ARID1B):c.1032_1034GGC[5] (p.Ala350dup) rs764418312
NM_017519.2(ARID1B):c.1041_1046dup (p.Ala349_Ala350dup) rs1562377904
NM_017519.2(ARID1B):c.1043_1045CAG[4] (p.Ala350dup) rs797045267
NM_017519.2(ARID1B):c.1043_1045CAG[5] (p.Ala349_Ala350dup) rs797045267
NM_017519.2(ARID1B):c.1054_1056GGC[4] (p.Gly356_Gly357del) rs797045268
NM_017519.2(ARID1B):c.1054_1056GGC[5] (p.Gly357del) rs797045268
NM_017519.2(ARID1B):c.1054_1056GGC[7] (p.Gly357dup) rs797045268
NM_017519.2(ARID1B):c.1370_1372CGG[3] (p.Ala460del) rs757953295
NM_017519.2(ARID1B):c.1385_1387CGG[4] (p.Ala464dup) rs1367431735
NM_017519.2(ARID1B):c.1542+19G>C rs374013482
NM_017519.2(ARID1B):c.3306+11G>A rs368322992
NM_017519.2(ARID1B):c.4195T>G (p.Ser1399Ala) rs145516400
NM_017519.2(ARID1B):c.5506C>A (p.Pro1836Thr) rs779490460
NM_017519.2(ARID1B):c.6233T>C (p.Ile2078Thr) rs878852997
NM_017519.2(ARID1B):c.679_680delinsCC (p.Val227Pro) rs1554247605
NM_017519.2(ARID1B):c.921_923CGG[10] (p.Gly318_Gly319dup) rs587779747
NM_017519.2(ARID1B):c.921_923CGG[5] (p.Gly317_Gly319del) rs587779747
NM_017519.2(ARID1B):c.921_923CGG[6] (p.Gly318_Gly319del) rs587779747
NM_017519.2(ARID1B):c.921_923CGG[9] (p.Gly319dup) rs587779747
NM_017519.2(ARID1B):c.945_947AGG[5] (p.Gly319dup) rs587779748
NM_017519.2(ARID1B):c.962_964GAG[10] (p.Gly327_Gly328dup) rs747790383
NM_017519.2(ARID1B):c.962_964GAG[11] (p.Gly326_Gly328dup) rs747790383
NM_017519.2(ARID1B):c.962_964GAG[5] (p.Gly326_Gly328del) rs747790383
NM_017519.2(ARID1B):c.962_964GAG[6] (p.Gly327_Gly328del) rs747790383
NM_017519.2(ARID1B):c.962_964GAG[9] (p.Gly328dup) rs747790383
NM_017519.2(ARID1B):c.978_992AGGAGGAGCAGGAGC[1] (p.328_332GAGAG[1]) rs773423003
NM_017519.2(ARID1B):c.986_991CAGGAG[3] (p.329_330AG[3]) rs747438636
NM_017519.2(ARID1B):c.996_1001AGGAGC[3] (p.333_334GA[4]) rs1323804393
NM_020732.3(ARID1B):c.1088C>T (p.Ala363Val) rs748273011
NM_020732.3(ARID1B):c.1102C>T (p.Leu368=) rs1562378059
NM_020732.3(ARID1B):c.1329C>T (p.Pro443=) rs760419444
NM_020732.3(ARID1B):c.1592T>C (p.Met531Thr) rs141260832
NM_020732.3(ARID1B):c.1632G>A (p.Pro544=) rs142939952
NM_020732.3(ARID1B):c.1678A>G (p.Ile560Val) rs17318151
NM_020732.3(ARID1B):c.1714G>A (p.Gly572Arg) rs151093357
NM_020732.3(ARID1B):c.1737+28T>C rs73572289
NM_020732.3(ARID1B):c.1920G>A (p.Pro640=) rs374876774
NM_020732.3(ARID1B):c.1932G>A (p.Met644Ile) rs142897795
NM_020732.3(ARID1B):c.1977C>T (p.Pro659=) rs146240413
NM_020732.3(ARID1B):c.2038-35G>A rs3734440
NM_020732.3(ARID1B):c.2070G>A (p.Thr690=) rs201290874
NM_020732.3(ARID1B):c.2307C>T (p.Pro769=) rs541757080
NM_020732.3(ARID1B):c.2444C>T (p.Ser815Leu) rs150140314
NM_020732.3(ARID1B):c.2862G>C (p.Ala954=) rs148749268
NM_020732.3(ARID1B):c.2879+6C>T rs1203684217
NM_020732.3(ARID1B):c.2895C>T (p.Pro965=) rs144894118
NM_020732.3(ARID1B):c.2896G>A (p.Gly966Ser) rs34786733
NM_020732.3(ARID1B):c.2976G>T (p.Thr992=) rs755525381
NM_020732.3(ARID1B):c.2978A>T (p.Gln993Leu) rs139620600
NM_020732.3(ARID1B):c.3025+21C>T rs9397998
NM_020732.3(ARID1B):c.3025+38C>T rs9384530
NM_020732.3(ARID1B):c.3025+6C>T rs148976215
NM_020732.3(ARID1B):c.3120C>T (p.Pro1040=) rs752231248
NM_020732.3(ARID1B):c.3219C>T (p.Val1073=) rs371828409
NM_020732.3(ARID1B):c.3309C>T (p.Leu1103=) rs111368751
NM_020732.3(ARID1B):c.3312C>T (p.Tyr1104=) rs61736269
NM_020732.3(ARID1B):c.3399C>T (p.Thr1133=) rs142391292
NM_020732.3(ARID1B):c.3628C>G (p.Leu1210Val) rs138482029
NM_020732.3(ARID1B):c.3771C>T (p.Asn1257=) rs370523060
NM_020732.3(ARID1B):c.3796A>G (p.Met1266Val) rs773883674
NM_020732.3(ARID1B):c.3891G>C (p.Thr1297=) rs374823620
NM_020732.3(ARID1B):c.4071G>A (p.Pro1357=) rs374835455
NM_020732.3(ARID1B):c.4294A>G (p.Met1432Val) rs745566888
NM_020732.3(ARID1B):c.4305G>A (p.Pro1435=) rs566865279
NM_020732.3(ARID1B):c.4345G>A (p.Gly1449Ser) rs141461351
NM_020732.3(ARID1B):c.4440C>T (p.Gly1480=) rs139903653
NM_020732.3(ARID1B):c.4474G>A (p.Gly1492Ser) rs1274057762
NM_020732.3(ARID1B):c.4495A>T (p.Met1499Leu) rs34870395
NM_020732.3(ARID1B):c.4658C>T (p.Ala1553Val) rs762698567
NM_020732.3(ARID1B):c.4659G>A (p.Ala1553=) rs776881575
NM_020732.3(ARID1B):c.4671G>A (p.Ala1557=) rs374125873
NM_020732.3(ARID1B):c.4871G>A (p.Arg1624Gln) rs762183842
NM_020732.3(ARID1B):c.5015A>G (p.Asn1672Ser) rs140177120
NM_020732.3(ARID1B):c.5099A>G (p.Glu1700Gly) rs149841055
NM_020732.3(ARID1B):c.5289C>T (p.Ile1763=) rs533990759
NM_020732.3(ARID1B):c.5303C>T (p.Pro1768Leu) rs142466273
NM_020732.3(ARID1B):c.5307C>T (p.Asp1769=) rs537400492
NM_020732.3(ARID1B):c.5310C>T (p.Ala1770=) rs146982427
NM_020732.3(ARID1B):c.5311G>A (p.Ala1771Thr) rs768478175
NM_020732.3(ARID1B):c.5546C>G (p.Pro1849Arg) rs202194222
NM_020732.3(ARID1B):c.5607A>G (p.Gln1869=) rs1303216691
NM_020732.3(ARID1B):c.5650C>T (p.Arg1884Trp) rs1377877762
NM_020732.3(ARID1B):c.5694C>T (p.Thr1898=) rs376113162
NM_020732.3(ARID1B):c.5802C>T (p.Ile1934=) rs142499766
NM_020732.3(ARID1B):c.6072G>A (p.Thr2024=) rs371980859
NM_020732.3(ARID1B):c.6090C>T (p.Asn2030=) rs939615492
NM_020732.3(ARID1B):c.6294G>C (p.Leu2098=) rs1562354325
NM_020732.3(ARID1B):c.6342A>G (p.Thr2114=) rs147679171
NM_020732.3(ARID1B):c.640C>T (p.Pro214Ser) rs1301993972
NM_020732.3(ARID1B):c.6427G>A (p.Ala2143Thr) rs530084903
NM_020732.3(ARID1B):c.6504G>A (p.Thr2168=) rs377350616
NM_020732.3(ARID1B):c.6594G>A (p.Ala2198=) rs754242891
NM_020732.3(ARID1B):c.6642A>G (p.Glu2214=) rs756043689
NM_020732.3(ARID1B):c.6654C>T (p.His2218=) rs183572405
NM_020732.3(ARID1B):c.678C>T (p.Ala226=) rs1450163641
NM_020732.3(ARID1B):c.705C>T (p.Gly235=) rs745740327
NM_020732.3(ARID1B):c.714C>T (p.Ala238=) rs533517668
NM_020732.3(ARID1B):c.941_942insAGG (p.Gly319dup) rs1562377373
NM_020732.3(ARID1B):c.942C>A (p.Gly314=) rs184815562
NM_020732.3(ARID1B):c.945A>C (p.Gly315=) rs112474841
NM_020732.3(ARID1B):c.957_974del (p.Ser320_Gly325del) rs755976776
NM_020732.3:c.663C>T

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.