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Variant : CV455547 (NM_001271723.1(FBXO38):c.1265-7T>C) Homo sapiens

Symbol: CV455547
Name: NM_001271723.1(FBXO38):c.1265-7T>C
Condition: not provided [RCV000560881]
Clinical Significance: likely benign
Last Evaluated: 12/27/2018
Review Status: criteria provided, single submitter
Related Genes: FBXO38  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.148415921T>C
NC_000005.9:g.147795484T>C
NM_001271723.1:c.1265-7T>C
NG_033871.1:g.36987T>C
NM_030793.5:c.1265-7T>C
NM_205836.3:c.1265-7T>C
NM_030793.4:c.1265-7T>C
Position
Human AssemblyChrPosition (strand)Source
GRCh385148,415,921 - 148,415,921CLINVAR
GRCh375147,795,484 - 147,795,484CLINVAR
Cytogenetic Map55q32CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13497189
Created: 2018-01-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.