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

Variant : CV82983 (NM_018233.3(OGFOD1):c.225C>T (p.Phe75=)) Homo sapiens

Symbol: CV82983
Name: NM_018233.3(OGFOD1):c.225C>T (p.Phe75=)
Condition: Malignant melanoma [RCV000063063]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: NUDT21   OGFOD1  
Variant Type: single nucleotide variant (SO:0001636)
Source: CLINVAR
Molecular Consequence: synonymous variant|2kb upstream variant
Evidence: literature only|not provided
HGVS Name(s): NC_000016.8:g.55044746C>T
NM_018233.3:c.225C>T
NC_000016.10:g.56453333C>T
NC_000016.9:g.56487245C>T
NM_007006.2:c.-147-u1984G>A
NP_060703.3:p.Phe75=
NM_007006.2:c.-2131G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381656,453,333 - 56,453,333CLINVAR
GRCh371656,487,245 - 56,487,245CLINVAR
Build 361655,044,746 - 55,044,746CLINVAR
Cytogenetic Map1616q13CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8627839
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.