ClinVar Miner

List of variants in gene ALB reported as not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
NM_000477.7(ALB):c.1013A>G (p.Asp338Gly) rs76242087
NM_000477.7(ALB):c.1013A>T (p.Asp338Val) rs76242087
NM_000477.7(ALB):c.1195G>C (p.Asp399His) rs77514449
NM_000477.7(ALB):c.1275C>A (p.Tyr425Ter) rs281860283
NM_000477.7(ALB):c.1300C>T (p.Arg434Cys) rs78575701
NM_000477.7(ALB):c.1428+2T>C rs78784172
NM_000477.7(ALB):c.1610del (p.Ile537fs) rs77081291
NM_000477.7(ALB):c.1669G>A (p.Val557Met) rs78284052
NM_000477.7(ALB):c.166C>T (p.Gln56Ter) rs75470261
NM_000477.7(ALB):c.1721A>C (p.Asp574Ala) rs79738788
NM_000477.7(ALB):c.1750A>G (p.Lys584Glu) rs76671808
NM_000477.7(ALB):c.1786-15T>A rs78342924
NM_000477.7(ALB):c.1794dup (p.Leu599fs) rs75000326
NM_000477.7(ALB):c.228_229del (p.Val78fs) rs75152012
NM_000477.7(ALB):c.412C>T (p.Arg138Ter) rs77238412
NM_000477.7(ALB):c.437T>A (p.Val146Glu) rs77752336
NM_000477.7(ALB):c.597T>A (p.Ala199=) rs281860282
NM_000477.7(ALB):c.714G>A (p.Trp238Ter) rs76454301
NM_000477.7(ALB):c.802G>T (p.Glu268Ter) rs78340021

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.