ClinVar Miner

Submissions for variant NM_000155.4(GALT):c.377+2dup

gnomAD frequency: 0.00001  dbSNP: rs763662108
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001004334 SCV001163234 pathogenic Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001004334 SCV002955917 uncertain significance Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase 2022-05-27 criteria provided, single submitter clinical testing This sequence change falls in intron 4 of the GALT gene. It does not directly change the encoded amino acid sequence of the GALT protein. It affects a nucleotide within the consensus splice site. This variant is present in population databases (rs763662108, gnomAD 0.01%). This variant has been observed in individual(s) with intrahepatic cholestasis (PMID: 31450232). ClinVar contains an entry for this variant (Variation ID: 813411). Variants that disrupt the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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.