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Variant : CV87598 (NC_000007.14:g.142434295G>A) Homo sapiens

Symbol: CV87598
Name: NC_000007.14:g.142434295G>A
Condition: Malignant melanoma [RCV000067690]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: TRB   TRBV11-2  
Variant Type: single nucleotide variant (SO:0001483)
Source: CLINVAR
Evidence: literature only|not provided
HGVS Name(s): NC_000007.14:g.142434295G>A
NC_000007.13:g.142197669C>T
NC_000007.12:g.141802760G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh387142,434,295 - 142,434,295CLINVAR
GRCh377142,197,669 - 142,197,669CLINVAR
Build 367141,802,760 - 141,802,760CLINVAR
Cytogenetic Map77q34CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8632390
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.