ClinVar Miner

List of variants in gene ALDOB reported as likely benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 80
Download table as spreadsheet
HGVS dbSNP
NM_000035.4(ALDOB):c.*12C>T rs201867948
NM_000035.4(ALDOB):c.*152A>G
NM_000035.4(ALDOB):c.*567C>T rs540272117
NM_000035.4(ALDOB):c.*752C>G rs555999328
NM_000035.4(ALDOB):c.*849T>C rs181650438
NM_000035.4(ALDOB):c.1011G>A (p.Gln337=) rs566549564
NM_000035.4(ALDOB):c.1014G>A (p.Ala338=) rs546735701
NM_000035.4(ALDOB):c.1026G>A (p.Gln342=)
NM_000035.4(ALDOB):c.1035C>T (p.His345=) rs761508514
NM_000035.4(ALDOB):c.1044T>C (p.Ser348=)
NM_000035.4(ALDOB):c.1062C>G (p.Thr354=)
NM_000035.4(ALDOB):c.1065G>A (p.Gln355=)
NM_000035.4(ALDOB):c.1068G>A (p.Ser356=)
NM_000035.4(ALDOB):c.112+7G>A
NM_000035.4(ALDOB):c.178C>A (p.Arg60=) rs118204429
NM_000035.4(ALDOB):c.186C>T (p.Ile62=) rs1588172329
NM_000035.4(ALDOB):c.18A>T (p.Pro6=)
NM_000035.4(ALDOB):c.207C>T (p.Ser69=) rs779129856
NM_000035.4(ALDOB):c.222C>T (p.Ile74=)
NM_000035.4(ALDOB):c.231G>T (p.Val77=)
NM_000035.4(ALDOB):c.243C>T (p.His81=) rs182003715
NM_000035.4(ALDOB):c.249C>T (p.Thr83=)
NM_000035.4(ALDOB):c.252C>G (p.Leu84=)
NM_000035.4(ALDOB):c.264C>A (p.Asp88Glu) rs200585150
NM_000035.4(ALDOB):c.282C>T (p.Phe94=) rs549682194
NM_000035.4(ALDOB):c.285A>G (p.Arg95=)
NM_000035.4(ALDOB):c.294C>G (p.Leu98=)
NM_000035.4(ALDOB):c.318A>G (p.Gly106=)
NM_000035.4(ALDOB):c.324+7A>C
NM_000035.4(ALDOB):c.336A>C (p.Gly112=) rs1248064943
NM_000035.4(ALDOB):c.369C>A (p.Thr123=)
NM_000035.4(ALDOB):c.375T>C (p.Ile125=) rs886063292
NM_000035.4(ALDOB):c.380-4G>T
NM_000035.4(ALDOB):c.396A>G (p.Ser132=)
NM_000035.4(ALDOB):c.423T>C (p.Asp141=)
NM_000035.4(ALDOB):c.462T>C (p.Ile154=)
NM_000035.4(ALDOB):c.465C>A (p.Ala155=)
NM_000035.4(ALDOB):c.465C>T (p.Ala155=) rs569981883
NM_000035.4(ALDOB):c.468C>T (p.Asp156=)
NM_000035.4(ALDOB):c.480C>T (p.Ser160=)
NM_000035.4(ALDOB):c.486C>G (p.Leu162=)
NM_000035.4(ALDOB):c.486C>T (p.Leu162=) rs773334784
NM_000035.4(ALDOB):c.489T>A (p.Ala163=) rs578048957
NM_000035.4(ALDOB):c.501C>T (p.Asn167=) rs186836225
NM_000035.4(ALDOB):c.507C>T (p.Asn169=) rs746351347
NM_000035.4(ALDOB):c.511C>T (p.Leu171=)
NM_000035.4(ALDOB):c.522C>T (p.Tyr174=) rs752902486
NM_000035.4(ALDOB):c.525C>T (p.Ala175=) rs144196914
NM_000035.4(ALDOB):c.537G>A (p.Gln179=) rs775053176
NM_000035.4(ALDOB):c.540+9C>A
NM_000035.4(ALDOB):c.543T>G (p.Asn181Lys) rs35885472
NM_000035.4(ALDOB):c.549G>T (p.Leu183=)
NM_000035.4(ALDOB):c.582T>C (p.Asp194=) rs141988626
NM_000035.4(ALDOB):c.619G>C (p.Glu207Gln) rs3739721
NM_000035.4(ALDOB):c.621G>A (p.Glu207=)
NM_000035.4(ALDOB):c.625-10T>C
NM_000035.4(ALDOB):c.654T>C (p.Asn218=) rs780943027
NM_000035.4(ALDOB):c.681C>T (p.Thr227=) rs61757689
NM_000035.4(ALDOB):c.690G>A (p.Lys230=)
NM_000035.4(ALDOB):c.708T>C (p.Ala236=)
NM_000035.4(ALDOB):c.717C>T (p.Ala239=) rs772197524
NM_000035.4(ALDOB):c.738A>G (p.Pro246=)
NM_000035.4(ALDOB):c.750T>A (p.Ala250=)
NM_000035.4(ALDOB):c.759C>A (p.Thr253=) rs146360505
NM_000035.4(ALDOB):c.799+11C>T rs182245025
NM_000035.4(ALDOB):c.799+6G>A rs141888548
NM_000035.4(ALDOB):c.800-5A>G
NM_000035.4(ALDOB):c.800-6T>C
NM_000035.4(ALDOB):c.813G>A (p.Leu271=)
NM_000035.4(ALDOB):c.819T>C (p.Gly273=)
NM_000035.4(ALDOB):c.849C>T (p.Asn283=) rs202062631
NM_000035.4(ALDOB):c.873T>A (p.Pro291=) rs765247994
NM_000035.4(ALDOB):c.906T>C (p.Tyr302=) rs138866018
NM_000035.4(ALDOB):c.912G>C (p.Arg304=)
NM_000035.4(ALDOB):c.915C>G (p.Ala305=)
NM_000035.4(ALDOB):c.933G>A (p.Leu311=)
NM_000035.4(ALDOB):c.954T>C (p.Ala318=) rs572044496
NM_000035.4(ALDOB):c.966G>A (p.Glu322=) rs149166711
NM_000035.4(ALDOB):c.996C>T (p.Ala332=)
NM_000035.4(ALDOB):c.99A>C (p.Ala33=)

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.