ClinVar Miner

List of variants in gene ALB reported by OMIM

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Gene type:
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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_000477.7(ALB):c.1195G>A (p.Asp399Asn) rs77514449 0.00016
NM_000477.7(ALB):c.1721A>G (p.Asp574Gly) rs79738788 0.00012
NM_000477.7(ALB):c.1011G>T (p.Lys337Asn) rs72552710 0.00011
NM_000477.5(ALB):c.67C>T (p.Arg23Cys) rs80008208 0.00009
NM_000477.7(ALB):c.725G>A (p.Arg242His) rs75002628 0.00008
NM_000477.7(ALB):c.1759G>A (p.Asp587Asn) rs76587671 0.00006
NM_000477.7(ALB):c.79C>T (p.His27Tyr) rs141733599 0.00006
NM_000477.7(ALB):c.1144G>A (p.Glu382Lys) rs75791663 0.00002
NM_000477.7(ALB):c.1552G>A (p.Asp518Asn) rs75920790 0.00002
NM_000477.7(ALB):c.412C>T (p.Arg138Ter) rs77238412 0.00002
NM_000477.5(ALB):c.71G>A (p.Arg24Gln) rs74821926 0.00001
NM_000477.7(ALB):c.1166A>T (p.Asp389Val) rs78538497 0.00001
NM_000477.7(ALB):c.1186A>G (p.Lys396Glu) rs78166690 0.00001
NM_000477.7(ALB):c.1198G>C (p.Glu400Gln) rs79047363 0.00001
NM_000477.7(ALB):c.1693A>G (p.Lys565Glu) rs80345158 0.00001
NM_000477.7(ALB):c.1789A>G (p.Lys597Glu) rs80106970 0.00001
NM_000477.7(ALB):c.1810del (p.Gln604fs) rs77158239 0.00001
NM_000477.7(ALB):c.68G>A (p.Arg23His) rs72552709 0.00001
NM_000477.7(ALB):c.79+1G>A rs77408163 0.00001
NM_000477.7(ALB):c.790A>G (p.Lys264Glu) rs79377490 0.00001
NM_000477.7(ALB):c.900G>C (p.Lys300Asn) rs74718349 0.00001
NM_000477.5(ALB):c.71G>C (p.Arg24Pro) rs74821926
NM_000477.5(ALB):c.71G>T (p.Arg24Leu) rs74821926
NM_000477.7(ALB):c.1026C>G (p.Asn342Lys) rs77544362
NM_000477.7(ALB):c.1033G>A (p.Glu345Lys) rs72552711
NM_000477.7(ALB):c.1069G>A (p.Glu357Lys) rs77354753
NM_000477.7(ALB):c.1098dup (p.Val367fs) rs1577939845
NM_000477.7(ALB):c.1132G>A (p.Glu378Lys) rs76593094
NM_000477.7(ALB):c.1165G>C (p.Asp389His) rs77187142
NM_000477.7(ALB):c.1198G>A (p.Glu400Lys) rs79047363
NM_000477.7(ALB):c.1216G>A (p.Glu406Lys) rs76483862
NM_000477.7(ALB):c.1507G>A (p.Glu503Lys) rs80259813
NM_000477.7(ALB):c.1573G>A (p.Glu525Lys) rs75523493
NM_000477.7(ALB):c.1585G>A (p.Glu529Lys) rs74826639
NM_000477.7(ALB):c.166C>T (p.Gln56Ter) rs75470261
NM_000477.7(ALB):c.1678A>G (p.Lys560Glu) rs77645174
NM_000477.7(ALB):c.1765G>A (p.Glu589Lys) rs75709682
NM_000477.7(ALB):c.1771del (p.Cys591fs) rs74674594
NM_000477.7(ALB):c.1780G>A (p.Glu594Lys) rs79228041
NM_000477.7(ALB):c.1785+1G>C rs1800580
NM_000477.7(ALB):c.1794A>Y (p.Lys598Asn) rs75738598
NM_000477.7(ALB):c.1825_*23+1delinsAAAAT
NM_000477.7(ALB):c.250G>A (p.Glu84Lys) rs77050410
NM_000477.7(ALB):c.259G>A (p.Asp87Asn) rs78574148
NM_000477.7(ALB):c.269T>C (p.Leu90Pro) rs77892378
NM_000477.7(ALB):c.316G>A (p.Glu106Lys) rs80296402
NM_000477.7(ALB):c.412C>G (p.Arg138Gly) rs77238412
NM_000477.7(ALB):c.427G>A (p.Glu143Lys) rs75522063
NM_000477.7(ALB):c.455A>G (p.His152Arg) rs80095457
NM_000477.7(ALB):c.491A>G (p.Tyr164Cys) rs78283180
NM_000477.7(ALB):c.602G>T (p.Cys201Phe) rs77656691
NM_000477.7(ALB):c.714-2A>G rs77335374
NM_000477.7(ALB):c.714G>A (p.Trp238Ter) rs76454301
NM_000477.7(ALB):c.725G>C (p.Arg242Pro) rs75002628
NM_000477.7(ALB):c.745A>C (p.Lys249Gln) rs79804069
NM_000477.7(ALB):c.74A>T (p.Asp25Val) rs75353611
NM_000477.7(ALB):c.81C>R (p.His27Gln) rs76285851
NM_000477.7(ALB):c.872dup (p.Asn291fs) rs77449454
NM_000477.7(ALB):c.875A>G (p.Gln292Arg) rs80002911
NM_000477.7(ALB):c.878A>G (p.Asp293Gly) rs79744198
NM_000477.7(ALB):c.[1030G>A;67C>T]

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