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Variant : CV307419 (NM_014780.4(CUL7):c.4683G>A (p.Glu1561=)) Homo sapiens

Symbol: CV307419
Name: NM_014780.4(CUL7):c.4683G>A (p.Glu1561=)
Condition: Three M syndrome [RCV000377546]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: CUL7  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NM_014780.4:c.4683G>A
NG_016205.1:g.20589G>A
NC_000006.12:g.43038357C>T
NC_000006.11:g.43006095C>T
NP_055595.2:p.Glu1561=
Position
Human AssemblyChrPosition (strand)Source
GRCh38643,038,357 - 43,038,357CLINVAR
GRCh37643,006,095 - 43,006,095CLINVAR
Cytogenetic Map66p21.1CLINVAR



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11661535
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-08-06
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.