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Variant : CV89718 (NM_152591.2(CCDC63):c.1067G>A (p.Arg356Gln)) Homo sapiens

Symbol: CV89718
Name: NM_152591.2(CCDC63):c.1067G>A (p.Arg356Gln)
Condition: Malignant melanoma [RCV000069815]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: CCDC63  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NC_000012.12:g.110884243G>A
NC_000012.11:g.111322047G>A
NM_152591.2:c.1067G>A
NM_152591.1:c.1067G>A
NP_689804.1:p.Arg356Gln
NC_000012.10:g.109806430G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh3812110,884,243 - 110,884,243CLINVAR
GRCh3712111,322,047 - 111,322,047CLINVAR
Build 3612109,806,430 - 109,806,430CLINVAR
Cytogenetic Map1212q24.11CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8634498
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.