ClinVar Miner

List of variants in gene SCARB2 reported as uncertain significance for Unverricht-Lundborg syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP
NC_000004.11:g.(?_77082846)_(77102274_?)dup
NC_000004.11:g.(?_77116840)_(77134716_?)dup
NM_005506.4(SCARB2):c.1010T>C (p.Met337Thr) rs147324129
NM_005506.4(SCARB2):c.1057A>G (p.Ile353Val)
NM_005506.4(SCARB2):c.1067T>C (p.Met356Thr)
NM_005506.4(SCARB2):c.1136C>T (p.Ala379Val) rs144147706
NM_005506.4(SCARB2):c.117G>A (p.Lys39=)
NM_005506.4(SCARB2):c.1194G>A (p.Thr398=) rs574498998
NM_005506.4(SCARB2):c.11G>A (p.Cys4Tyr) rs1196467385
NM_005506.4(SCARB2):c.1210A>G (p.Met404Val)
NM_005506.4(SCARB2):c.1229A>T (p.Tyr410Phe) rs777270813
NM_005506.4(SCARB2):c.1235A>G (p.Asn412Ser) rs771661901
NM_005506.4(SCARB2):c.1239+8C>G rs369265725
NM_005506.4(SCARB2):c.1262C>T (p.Thr421Met) rs149474488
NM_005506.4(SCARB2):c.1265C>T (p.Ala422Val) rs756606813
NM_005506.4(SCARB2):c.1271G>A (p.Arg424Gln) rs751827409
NM_005506.4(SCARB2):c.1302C>G (p.Ile434Met)
NM_005506.4(SCARB2):c.1327A>G (p.Met443Val)
NM_005506.4(SCARB2):c.1328T>C (p.Met443Thr) rs141250135
NM_005506.4(SCARB2):c.1373G>T (p.Cys458Phe)
NM_005506.4(SCARB2):c.1382_1383del (p.Gln461fs) rs1233094134
NM_005506.4(SCARB2):c.1412A>T (p.Glu471Val)
NM_005506.4(SCARB2):c.194A>G (p.Tyr65Cys) rs138955932
NM_005506.4(SCARB2):c.223A>T (p.Ile75Phe) rs1560716099
NM_005506.4(SCARB2):c.244C>T (p.Arg82Trp) rs142690468
NM_005506.4(SCARB2):c.277G>A (p.Glu93Lys) rs145870223
NM_005506.4(SCARB2):c.280C>T (p.Leu94Phe) rs752416481
NM_005506.4(SCARB2):c.379G>T (p.Asp127Tyr) rs148022786
NM_005506.4(SCARB2):c.381C>G (p.Asp127Glu) rs1553948511
NM_005506.4(SCARB2):c.382C>T (p.Pro128Ser) rs143558324
NM_005506.4(SCARB2):c.443A>G (p.Gln148Arg) rs1560710284
NM_005506.4(SCARB2):c.463A>G (p.Ile155Val) rs772434203
NM_005506.4(SCARB2):c.515C>T (p.Thr172Ile)
NM_005506.4(SCARB2):c.638A>T (p.Tyr213Phe) rs751953388
NM_005506.4(SCARB2):c.705-7A>G
NM_005506.4(SCARB2):c.746A>G (p.Asn249Ser) rs199837910
NM_005506.4(SCARB2):c.752C>T (p.Thr251Ile) rs1553948166
NM_005506.4(SCARB2):c.80G>A (p.Arg27Gln) rs368906199
NM_005506.4(SCARB2):c.825-3C>T
NM_005506.4(SCARB2):c.851A>C (p.Tyr284Ser) rs149997095
NM_005506.4(SCARB2):c.869T>A (p.Leu290Gln) rs1553948019
NM_005506.4(SCARB2):c.903A>G (p.Ile301Met) rs1485497925
NM_005506.4(SCARB2):c.911A>G (p.Asn304Ser) rs150870503
NM_005506.4(SCARB2):c.919G>A (p.Asp307Asn) rs142392473
NM_005506.4(SCARB2):c.962C>T (p.Ser321Leu) rs1553947990
NM_005506.4(SCARB2):c.9A>G (p.Arg3=) rs148558907

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.