ClinVar Miner

List of variants in gene ALB reported as not provided

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Total variants: 19
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HGVS dbSNP
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

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