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

Variant : CV90015 (NM_003920.3(TIMELESS):c.3262C>T (p.Pro1088Ser)) Homo sapiens

Symbol: CV90015
Name: NM_003920.3(TIMELESS):c.3262C>T (p.Pro1088Ser)
Condition: Malignant melanoma [RCV000070112]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: TIMELESS  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NM_003920.3:c.3262C>T
NC_000012.12:g.56418326G>A
NC_000012.11:g.56812110G>A
NM_003920.2:c.3262C>T
NP_003911.2:p.Pro1088Ser
NC_000012.10:g.55098377G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381256,418,326 - 56,418,326CLINVAR
GRCh371256,812,110 - 56,812,110CLINVAR
Build 361255,098,377 - 55,098,377CLINVAR
Cytogenetic Map1212q13.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8634795
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.