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Variant : CV312566 (NM_001497.3(B4GALT1):c.*705dup) Homo sapiens

Symbol: CV312566
Name: NM_001497.3(B4GALT1):c.*705dup
Condition: Congenital disorder of glycosylation [RCV000317423]
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.59610dup
NM_001497.3:c.*705dup
NC_000009.12:g.33112757dup
NC_000009.11:g.33112755dup
NM_001497.3:c.*705dupT
Position
Human AssemblyChrPosition (strand)Source
GRCh38933,112,748 - 33,112,749CLINVAR
GRCh37933,112,746 - 33,112,747CLINVAR
Cytogenetic Map99p21.1CLINVAR
Trait Synonyms: Carbohydrate-deficient glycoprotein syndrome



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11635182
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.