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

Variant : CV83355 (NM_052850.3(GADD45GIP1):c.183C>T (p.Phe61=)) Homo sapiens

Symbol: CV83355
Name: NM_052850.3(GADD45GIP1):c.183C>T (p.Phe61=)
Condition: Malignant melanoma [RCV000063435]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: GADD45GIP1   RAD23A  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NC_000019.8:g.12928844G>A
NC_000019.10:g.12957030G>A
NC_000019.9:g.13067844G>A
NM_005053.2:c.*592+d3389G>A
NM_052850.3:c.183C>T
NM_052850.2:c.183C>T
NP_443082.2:p.Phe61=
Position
Human AssemblyChrPosition (strand)Source
GRCh381912,957,030 - 12,957,030CLINVAR
GRCh371913,067,844 - 13,067,844CLINVAR
Build 361912,928,844 - 12,928,844CLINVAR
Cytogenetic Map1919p13.13CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8628211
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
Status: ACTIVE



NHLBI Logo

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