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Variant : CV318946 (NM_001497.3(B4GALT1):c.*1087dup) Homo sapiens

Symbol: CV318946
Name: NM_001497.3(B4GALT1):c.*1087dup
Condition: Congenital disorder of glycosylation [RCV000393571]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: B4GALT1  
Variant Type: duplication (SO:0001624)
Source: CLINVAR
Molecular Consequence: 3 prime utr variant
Evidence: clinical testing
HGVS Name(s): NG_008919.1:g.59992dup
NM_001497.3:c.*1087dup
NC_000009.12:g.33112368dup
NC_000009.11:g.33112366dup
NM_001497.3:c.*1087dupC
Position
Human AssemblyChrPosition (strand)Source
GRCh38933,112,366 - 33,112,367CLINVAR
GRCh37933,112,364 - 33,112,365CLINVAR
Cytogenetic Map99p21.1CLINVAR
Trait Synonyms: Carbohydrate-deficient glycoprotein syndrome



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11635763
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2020-10-15
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.