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

Variant : CV269732 (NM_014780.4(CUL7):c.2644C>T (p.Arg882Trp)) Homo sapiens

Symbol: CV269732
Name: NM_014780.4(CUL7):c.2644C>T (p.Arg882Trp)
Condition: not specified [RCV000305787]
Clinical Significance: uncertain significance
Last Evaluated: 01/12/2016
Review Status: criteria provided, single submitter
Related Genes: CUL7  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NM_014780.4:c.2644C>T
NG_016205.1:g.12694C>T
NC_000006.12:g.43046252G>A
NC_000006.11:g.43013990G>A
NP_055595.2:p.Arg882Trp
Position
Human AssemblyChrPosition (strand)Source
GRCh38643,046,252 - 43,046,252CLINVAR
GRCh37643,013,990 - 43,013,990CLINVAR
Cytogenetic Map66p21.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11638546
Created: 2017-01-11
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.