Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV491765 (NM_014780.4(CUL7):c.2901A>G (p.Leu967=)) Homo sapiens

Symbol: CV491765
Name: NM_014780.4(CUL7):c.2901A>G (p.Leu967=)
Condition: not specified [RCV000592716]
Clinical Significance: uncertain significance
Last Evaluated: 02/20/2017
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.2901A>G
NG_016205.1:g.13582A>G
NC_000006.12:g.43045364T>C
NC_000006.11:g.43013102T>C
NP_055595.2:p.Leu967=
Position
Human AssemblyChrPosition (strand)Source
GRCh38643,045,364 - 43,045,364CLINVAR
GRCh37643,013,102 - 43,013,102CLINVAR
Cytogenetic Map66p21.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13523214
Created: 2018-04-10
Species: Homo sapiens
Last Modified: 2019-08-06
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.