ClinVar Miner

List of variants in gene MBD5 reported as pathogenic for autosomal anomaly

Included ClinVar conditions (123):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
MBD5, THR157GLNFSTER4
NC_000002.11:g.(?_149216328)_(149221508_?)dup
NC_000002.11:g.(?_149216328)_(149228050_?)del
NC_000002.12:g.(?_148458739)_(148463939_?)del
NC_000002.12:g.(?_148458739)_(148512961_?)del
NC_000002.12:g.(?_148458759)_(148512941_?)del
NG_017003.3:g.262835_474705del
NM_001378120.1(MBD5):c.1000del (p.Gln334fs) rs1574459612
NM_001378120.1(MBD5):c.1023_1024delinsGA (p.Pro342Thr)
NM_001378120.1(MBD5):c.1025dup (p.Ser343fs) rs1553518511
NM_001378120.1(MBD5):c.1188del (p.Met396fs) rs2105630210
NM_001378120.1(MBD5):c.1379C>A (p.Ser460Ter) rs878910680
NM_001378120.1(MBD5):c.143del (p.Glu48fs) rs2105571301
NM_001378120.1(MBD5):c.1449del (p.Ser484fs) rs2105633124
NM_001378120.1(MBD5):c.1499_1500dup (p.Arg501fs) rs2105633619
NM_001378120.1(MBD5):c.14_15del (p.Lys5fs)
NM_001378120.1(MBD5):c.150del (p.Thr52fs) rs398122412
NM_001378120.1(MBD5):c.1648del (p.Ser550fs) rs2105635449
NM_001378120.1(MBD5):c.1759C>T (p.Gln587Ter) rs1559087186
NM_001378120.1(MBD5):c.180C>A (p.Cys60Ter) rs2105571544
NM_001378120.1(MBD5):c.188dup (p.Glu65fs)
NM_001378120.1(MBD5):c.196dup (p.Cys66fs)
NM_001378120.1(MBD5):c.2113del (p.Leu705fs) rs2105639771
NM_001378120.1(MBD5):c.217-1G>C rs1707171202
NM_001378120.1(MBD5):c.2299_2302del (p.Asn767fs) rs1060501153
NM_001378120.1(MBD5):c.2321del (p.Pro774fs) rs1553518752
NM_001378120.1(MBD5):c.2356C>T (p.Gln786Ter) rs2105642195
NM_001378120.1(MBD5):c.2437C>T (p.Gln813Ter) rs1057524832
NM_001378120.1(MBD5):c.2586_2667del (p.Ser863fs) rs1559094754
NM_001378120.1(MBD5):c.2633del (p.Pro878fs) rs1553519853
NM_001378120.1(MBD5):c.3572del (p.Thr1190_Leu1191insTer) rs2105093302
NM_001378120.1(MBD5):c.3598C>T (p.Gln1200Ter)
NM_001378120.1(MBD5):c.3598del (p.Gln1200fs)
NM_001378120.1(MBD5):c.3726_3729dup (p.Ala1244fs)
NM_001378120.1(MBD5):c.3769del (p.Asp1257fs) rs2105123510
NM_001378120.1(MBD5):c.3790A>T (p.Arg1264Ter) rs1450731543
NM_001378120.1(MBD5):c.379del (p.Ser127fs) rs1553517984
NM_001378120.1(MBD5):c.3828dup (p.Asn1277fs) rs2105124073
NM_001378120.1(MBD5):c.3907C>T (p.Gln1303Ter) rs2105124818
NM_001378120.1(MBD5):c.397+1G>A rs1553517991
NM_001378120.1(MBD5):c.397+2T>C
NM_001378120.1(MBD5):c.4429C>T (p.Gln1477Ter) rs1681473896
NM_001378120.1(MBD5):c.4585C>T (p.Arg1529Ter) rs2105130509
NM_001378120.1(MBD5):c.469_476del (p.Thr157fs) rs2105622677
NM_001378120.1(MBD5):c.4704_4728dup (p.Ser1577delinsLeuGlnTrpArgLeuTer)
NM_001378120.1(MBD5):c.4729del (p.Ser1577fs) rs2105131625
NM_001378120.1(MBD5):c.4765_4766insGGCACACACA (p.Lys1589fs)
NM_001378120.1(MBD5):c.4868G>A (p.Trp1623Ter)
NM_001378120.1(MBD5):c.4869G>A (p.Trp1623Ter)
NM_001378120.1(MBD5):c.4934C>A (p.Ser1645Ter) rs1559099927
NM_001378120.1(MBD5):c.4946del (p.Ser1649fs)
NM_001378120.1(MBD5):c.5154del (p.Lys1719fs) rs1060501151
NM_001378120.1(MBD5):c.535_547del (p.Gly179fs) rs1680665652
NM_001378120.1(MBD5):c.598C>T (p.Arg200Ter) rs1293936199
NM_001378120.1(MBD5):c.598dup (p.Arg200fs)
NM_001378120.1(MBD5):c.698del (p.Gly233fs) rs1680673822
NM_001378120.1(MBD5):c.707C>G (p.Ser236Ter) rs766179352
NM_001378120.1(MBD5):c.710_725del (p.Ile237fs) rs2105625178
NM_001378120.1(MBD5):c.728del (p.Pro243fs) rs1680676671
NM_001378120.1(MBD5):c.74G>A (p.Trp25Ter)
NM_001378120.1(MBD5):c.76C>T (p.Gln26Ter)
NM_001378120.1(MBD5):c.947del (p.Asn316fs) rs1680684706

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.