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Variant : CV348141 (NM_000528.4(MAN2B1):c.1398G>A (p.Ala466=)) Homo sapiens

Symbol: CV348141
Name: NM_000528.4(MAN2B1):c.1398G>A (p.Ala466=)
Condition: Deficiency of alpha-mannosidase [RCV000392764]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: MAN2B1  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NP_001166969.1:p.Ala465=
NG_008318.1:g.14311G>A
NC_000019.10:g.12657467C>T
NC_000019.9:g.12768281C>T
NP_000519.2:p.Ala466=
NM_001173498.1:c.1395G>A
NM_000528.4:c.1398G>A
NM_000528.3:c.1398G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381912,657,467 - 12,657,467CLINVAR
GRCh371912,768,281 - 12,768,281CLINVAR
Cytogenetic Map1919p13.13CLINVAR
Trait Synonyms: Alpha-Mannosidosis
Age Of Onset: childhood
Prevalence: 1-9 / 1 000 000



Disease Annotations

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11665167
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.