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Variant : CV312539 (NM_001497.3(B4GALT1):c.*2759T>G) Homo sapiens

Symbol: CV312539
Name: NM_001497.3(B4GALT1):c.*2759T>G
Condition: Congenital disorder of glycosylation [RCV000331485]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: B4GALT1  
Variant Type: single nucleotide variant (SO:0001624)
Source: CLINVAR
Molecular Consequence: 3 prime utr variant
Evidence: clinical testing
HGVS Name(s): NM_001497.3:c.*2759T>G
NG_008919.1:g.61664T>G
NC_000009.12:g.33110695A>C
NC_000009.11:g.33110693A>C
Position
Human AssemblyChrPosition (strand)Source
GRCh38933,110,695 - 33,110,695CLINVAR
GRCh37933,110,693 - 33,110,693CLINVAR
Cytogenetic Map99p21.1CLINVAR
Trait Synonyms: Carbohydrate-deficient glycoprotein syndrome



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11606435
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-11-12
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.