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Variant : CV778060 (NM_001079537.2(TRAPPC6B):c.352-16dup) Homo sapiens

Symbol: CV778060
Name: NM_001079537.2(TRAPPC6B):c.352-16dup
Condition: not provided [RCV000951309]
Clinical Significance: benign
Last Evaluated: 07/26/2018
Review Status: criteria provided, single submitter
Related Genes: TRAPPC6B  
Variant Type: duplication (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NM_177452.4:c.268-16dup
NM_001079537.2:c.352-16dup
NC_000014.9:g.39151848dup
NC_000014.9:g.39151855dup
NC_000014.8:g.39621059dup
NM_001079537.1:c.352-9dupT
Position
Human AssemblyChrPosition (strand)Source
GRCh381439,151,847 - 39,151,848CLINVAR
GRCh371439,621,051 - 39,621,052CLINVAR
Cytogenetic Map1414q21.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 15178562
Created: 2020-01-07
Species: Homo sapiens
Last Modified: 2020-02-11
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.