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Variant : CV90351 (NC_000014.9:g.106874737C>T) Homo sapiens

Symbol: CV90351
Name: NC_000014.9:g.106874737C>T
Condition: Malignant melanoma [RCV000070449]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: IGH   IGHV7-81  
Variant Type: single nucleotide variant (SO:0001483)
Source: CLINVAR
Evidence: literature only|not provided
HGVS Name(s): NC_000014.7:g.106353991C>T
NC_000014.9:g.106874737C>T
NC_000014.8:g.107282946C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh3814106,874,737 - 106,874,737CLINVAR
GRCh3714107,282,946 - 107,282,946CLINVAR
Build 3614106,353,991 - 106,353,991CLINVAR
Cytogenetic Map1414q32.33CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8635129
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.