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Variant : CV88096 (NM_020427.2(SLURP1):c.10C>T (p.Arg4Cys)) Homo sapiens

Symbol: CV88096
Name: NM_020427.2(SLURP1):c.10C>T (p.Arg4Cys)
Condition: Malignant melanoma [RCV000068188]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: SLURP1  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NM_020427.2:c.10C>T
NG_011494.1:g.5036C>T
NC_000008.11:g.142742376G>A
NC_000008.10:g.143823794G>A
NP_065160.1:p.Arg4Cys
NC_000008.9:g.143820796G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh388142,742,376 - 142,742,376CLINVAR
GRCh378143,823,794 - 143,823,794CLINVAR
Build 368143,820,796 - 143,820,796CLINVAR
Cytogenetic Map88q24.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8632881
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.