ClinVar Miner

List of variants in gene PRDM8 reported as likely benign for childhood-onset epilepsy syndrome

Included ClinVar conditions (90):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 123
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001099403.2(PRDM8):c.1314C>T (p.Ala438=) rs188061449 0.01796
NM_001099403.2(PRDM8):c.1407G>A (p.Ala469=) rs559035384 0.00075
NM_001099403.2(PRDM8):c.910G>C (p.Gly304Arg) rs747934880 0.00048
NM_001099403.2(PRDM8):c.1333C>T (p.Leu445=) rs951714195 0.00030
NM_001099403.2(PRDM8):c.219+17G>A rs374010085 0.00012
NM_001099403.2(PRDM8):c.1779_1796del (p.Ala594_Gly599del) rs574748973 0.00009
NM_001099403.2(PRDM8):c.90C>T (p.Tyr30=) rs767896746 0.00009
NM_001099403.2(PRDM8):c.1647C>T (p.Leu549=) rs770130991 0.00007
NM_001099403.2(PRDM8):c.858T>C (p.Gly286=) rs920460933 0.00006
NM_001099403.2(PRDM8):c.2040C>T (p.His680=) rs376730468 0.00005
NM_001099403.2(PRDM8):c.1236G>A (p.Glu412=) rs1296620793 0.00004
NM_001099403.2(PRDM8):c.1239C>T (p.Asp413=) rs955890394 0.00004
NM_001099403.2(PRDM8):c.1569C>G (p.Leu523=) rs771399439 0.00004
NM_001099403.2(PRDM8):c.750C>G (p.Ala250=) rs1458732519 0.00004
NM_001099403.2(PRDM8):c.774C>T (p.Ser258=) rs1477843578 0.00004
NM_001099403.2(PRDM8):c.885C>T (p.His295=) rs1031517706 0.00004
NM_001099403.2(PRDM8):c.1038G>A (p.Glu346=) rs752840771 0.00003
NM_001099403.2(PRDM8):c.1461C>G (p.Gly487=) rs766926830 0.00003
NM_001099403.2(PRDM8):c.663A>G (p.Leu221=) rs757742321 0.00003
NM_001099403.2(PRDM8):c.918C>T (p.Ala306=) rs777671444 0.00003
NM_001099403.2(PRDM8):c.1134G>A (p.Thr378=) rs944679589 0.00002
NM_001099403.2(PRDM8):c.1197G>A (p.Gln399=) rs1474812924 0.00002
NM_001099403.2(PRDM8):c.1035G>A (p.Lys345=) rs1192208565 0.00001
NM_001099403.2(PRDM8):c.1077C>T (p.Gly359=) rs746862284 0.00001
NM_001099403.2(PRDM8):c.1098G>A (p.Glu366=) rs1222924303 0.00001
NM_001099403.2(PRDM8):c.1215C>T (p.Asp405=) rs1560478454 0.00001
NM_001099403.2(PRDM8):c.1275C>T (p.Pro425=) rs1738619872 0.00001
NM_001099403.2(PRDM8):c.1306C>T (p.Leu436=) rs1321681007 0.00001
NM_001099403.2(PRDM8):c.1350G>A (p.Glu450=) rs1578265647 0.00001
NM_001099403.2(PRDM8):c.1396C>T (p.Leu466=) rs1738640851 0.00001
NM_001099403.2(PRDM8):c.1434G>C (p.Thr478=) rs1199927860 0.00001
NM_001099403.2(PRDM8):c.159C>T (p.Asp53=) rs1262983903 0.00001
NM_001099403.2(PRDM8):c.1674T>C (p.Gly558=) rs774459714 0.00001
NM_001099403.2(PRDM8):c.1764C>G (p.Ala588=) rs748241828 0.00001
NM_001099403.2(PRDM8):c.1767T>A (p.Ala589=) rs773515375 0.00001
NM_001099403.2(PRDM8):c.1809G>A (p.Leu603=) rs780466301 0.00001
NM_001099403.2(PRDM8):c.1821G>A (p.Ser607=) rs1361333573 0.00001
NM_001099403.2(PRDM8):c.1929T>C (p.His643=) rs761518640 0.00001
NM_001099403.2(PRDM8):c.1956T>C (p.Tyr652=) rs374015672 0.00001
NM_001099403.2(PRDM8):c.2043C>T (p.Leu681=) rs758880510 0.00001
NM_001099403.2(PRDM8):c.618C>G (p.Gly206=) rs370541374 0.00001
NM_001099403.2(PRDM8):c.660T>C (p.Pro220=) rs747489896 0.00001
NM_001099403.2(PRDM8):c.675C>G (p.Pro225=) rs749054601 0.00001
NM_001099403.2(PRDM8):c.1017G>T (p.Arg339=)
NM_001099403.2(PRDM8):c.1104C>T (p.Gly368=) rs1738591619
NM_001099403.2(PRDM8):c.1146G>A (p.Lys382=) rs2109879211
NM_001099403.2(PRDM8):c.1155C>T (p.Ala385=) rs2109879231
NM_001099403.2(PRDM8):c.1158C>T (p.Phe386=)
NM_001099403.2(PRDM8):c.1167G>C (p.Val389=) rs1276443060
NM_001099403.2(PRDM8):c.1167G>T (p.Val389=)
NM_001099403.2(PRDM8):c.1192C>T (p.Leu398=)
NM_001099403.2(PRDM8):c.1200G>A (p.Glu400=) rs2109879321
NM_001099403.2(PRDM8):c.1218C>G (p.Gly406=) rs2109879340
NM_001099403.2(PRDM8):c.1224A>G (p.Gly408=)
NM_001099403.2(PRDM8):c.1233C>G (p.Ser411=) rs2109879360
NM_001099403.2(PRDM8):c.1245C>T (p.Asp415=)
NM_001099403.2(PRDM8):c.1251C>A (p.Gly417=) rs1377717218
NM_001099403.2(PRDM8):c.1260C>G (p.Gly420=)
NM_001099403.2(PRDM8):c.1260C>T (p.Gly420=) rs1738615886
NM_001099403.2(PRDM8):c.1272G>A (p.Thr424=) rs1167938560
NM_001099403.2(PRDM8):c.1284G>A (p.Ala428=)
NM_001099403.2(PRDM8):c.1290G>A (p.Pro430=)
NM_001099403.2(PRDM8):c.1338C>T (p.Pro446=)
NM_001099403.2(PRDM8):c.1362T>G (p.Pro454=)
NM_001099403.2(PRDM8):c.1380C>T (p.Phe460=) rs2109879578
NM_001099403.2(PRDM8):c.1392G>T (p.Pro464=)
NM_001099403.2(PRDM8):c.1419C>T (p.Ser473=) rs1738644660
NM_001099403.2(PRDM8):c.1422T>G (p.Gly474=) rs1400958109
NM_001099403.2(PRDM8):c.1428C>A (p.Gly476=)
NM_001099403.2(PRDM8):c.1434G>A (p.Thr478=)
NM_001099403.2(PRDM8):c.1437C>A (p.Gly479=) rs904515362
NM_001099403.2(PRDM8):c.1446C>G (p.Ala482=) rs1578265921
NM_001099403.2(PRDM8):c.1446C>T (p.Ala482=) rs1578265921
NM_001099403.2(PRDM8):c.1461C>T (p.Gly487=)
NM_001099403.2(PRDM8):c.1611C>G (p.Leu537=)
NM_001099403.2(PRDM8):c.1638G>T (p.Ala546=)
NM_001099403.2(PRDM8):c.1659G>A (p.Ala553=) rs961379038
NM_001099403.2(PRDM8):c.1659G>C (p.Ala553=) rs961379038
NM_001099403.2(PRDM8):c.1665G>A (p.Leu555=)
NM_001099403.2(PRDM8):c.1668C>T (p.Asn556=) rs2109880238
NM_001099403.2(PRDM8):c.1671A>G (p.Gly557=) rs1287823085
NM_001099403.2(PRDM8):c.1677C>T (p.Cys559=) rs762021094
NM_001099403.2(PRDM8):c.1680G>A (p.Gly560=)
NM_001099403.2(PRDM8):c.1692C>T (p.Ser564=)
NM_001099403.2(PRDM8):c.1698C>G (p.Gly566=) rs1738695026
NM_001099403.2(PRDM8):c.1725C>T (p.Phe575=)
NM_001099403.2(PRDM8):c.1743C>T (p.Phe581=)
NM_001099403.2(PRDM8):c.1764C>T (p.Ala588=)
NM_001099403.2(PRDM8):c.1767T>C (p.Ala589=) rs773515375
NM_001099403.2(PRDM8):c.1782G>A (p.Ala594=) rs924936492
NM_001099403.2(PRDM8):c.1788G>C (p.Ala596=) rs752184496
NM_001099403.2(PRDM8):c.1812G>A (p.Gln604=) rs1553906523
NM_001099403.2(PRDM8):c.1833G>C (p.Leu611=)
NM_001099403.2(PRDM8):c.1839G>T (p.Pro613=)
NM_001099403.2(PRDM8):c.1845C>T (p.Ser615=)
NM_001099403.2(PRDM8):c.1875C>T (p.Asn625=)
NM_001099403.2(PRDM8):c.1881C>T (p.Cys627=)
NM_001099403.2(PRDM8):c.1884C>G (p.Ala628=) rs1738733654
NM_001099403.2(PRDM8):c.1950G>A (p.Lys650=)
NM_001099403.2(PRDM8):c.1959G>T (p.Ala653=)
NM_001099403.2(PRDM8):c.1968C>G (p.Pro656=) rs547453696
NM_001099403.2(PRDM8):c.1986A>G (p.Arg662=)
NM_001099403.2(PRDM8):c.2022C>T (p.Ser674=) rs765557090
NM_001099403.2(PRDM8):c.207G>A (p.Pro69=)
NM_001099403.2(PRDM8):c.219+13T>C
NM_001099403.2(PRDM8):c.219+17G>T
NM_001099403.2(PRDM8):c.564T>C (p.Ser188=)
NM_001099403.2(PRDM8):c.573C>T (p.Asp191=)
NM_001099403.2(PRDM8):c.57A>G (p.Gln19=) rs2109875602
NM_001099403.2(PRDM8):c.591G>T (p.Val197=)
NM_001099403.2(PRDM8):c.630A>G (p.Lys210=) rs1738515726
NM_001099403.2(PRDM8):c.633C>T (p.Asp211=)
NM_001099403.2(PRDM8):c.639G>A (p.Gln213=) rs749943042
NM_001099403.2(PRDM8):c.654G>A (p.Glu218=) rs1553905625
NM_001099403.2(PRDM8):c.666C>T (p.Gly222=)
NM_001099403.2(PRDM8):c.687A>G (p.Lys229=)
NM_001099403.2(PRDM8):c.747C>G (p.Ala249=) rs1578263531
NM_001099403.2(PRDM8):c.750C>T (p.Ala250=) rs1458732519
NM_001099403.2(PRDM8):c.798G>A (p.Arg266=) rs2109878495
NM_001099403.2(PRDM8):c.804G>A (p.Leu268=) rs1279908364
NM_001099403.2(PRDM8):c.81C>T (p.Thr27=)
NM_001099403.2(PRDM8):c.867C>T (p.Ser289=) rs750918327
NM_001099403.2(PRDM8):c.921G>C (p.Thr307=) rs770919711

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.