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Variant : CV86145 (NM_001813.2(CENPE):c.2310C>T (p.Leu770=)) Homo sapiens

Symbol: CV86145
Name: NM_001813.2(CENPE):c.2310C>T (p.Leu770=)
Condition: Malignant melanoma [RCV000066229]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: CENPE  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_001813.2:c.2310C>T
NC_000004.12:g.103159301G>A
NC_000004.11:g.104080458G>A
NP_001804.2:p.Leu770=
NG_041798.1:g.44109C>T
NC_000004.10:g.104299907G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh384103,159,301 - 103,159,301CLINVAR
GRCh374104,080,458 - 104,080,458CLINVAR
Build 364104,299,907 - 104,299,907CLINVAR
Cytogenetic Map44q24CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8630989
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.