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Variant : CV633580 (NM_205836.3(FBXO38):c.409G>A (p.Ala137Thr)) Homo sapiens

Symbol: CV633580
Name: NM_205836.3(FBXO38):c.409G>A (p.Ala137Thr)
Condition: Distal hereditary motor neuronopathy 2D [RCV000799608]
Clinical Significance: uncertain significance
Last Evaluated: 01/03/2019
Review Status: criteria provided, single submitter
Related Genes: FBXO38  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NM_001271723.1:c.409G>A
NM_030793.5:c.409G>A
NM_205836.3:c.409G>A
NG_033871.1:g.23194G>A
NC_000005.10:g.148402128G>A
NC_000005.9:g.147781691G>A
NM_030793.4:c.409G>A
NP_001258652.1:p.Ala137Thr
NP_110420.3:p.Ala137Thr
NP_995308.1:p.Ala137Thr
Position
Human AssemblyChrPosition (strand)Source
GRCh385148,402,128 - 148,402,128CLINVAR
GRCh375147,781,691 - 147,781,691CLINVAR
Cytogenetic Map55q32CLINVAR
Trait Synonyms: HMN IID; NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14727348
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2020-05-19
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.