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Variant : CV90017 (NM_003920.3(TIMELESS):c.829C>T (p.Arg277Ter)) Homo sapiens

Symbol: CV90017
Name: NM_003920.3(TIMELESS):c.829C>T (p.Arg277Ter)
Condition: Malignant melanoma [RCV000070114]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: TIMELESS  
Variant Type: single nucleotide variant (SO:0001587)
Source: CLINVAR
Molecular Consequence: stop-gain|nonsense
Evidence: literature only|not provided
HGVS Name(s): NM_003920.3:c.829C>T
NC_000012.12:g.56430961G>A
NC_000012.11:g.56824745G>A
NM_003920.2:c.829C>T
NP_003911.2:p.Arg277Ter
NC_000012.10:g.55111012G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381256,430,961 - 56,430,961CLINVAR
GRCh371256,824,745 - 56,824,745CLINVAR
Build 361255,111,012 - 55,111,012CLINVAR
Cytogenetic Map1212q13.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8634797
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
Status: ACTIVE



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