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Variant : CV82608 (NM_006418.4(OLFM4):c.1121C>T (p.Ser374Leu)) Homo sapiens

Symbol: CV82608
Name: NM_006418.4(OLFM4):c.1121C>T (p.Ser374Leu)
Condition: Malignant melanoma [RCV000062688]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: OLFM4  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NC_000013.9:g.52522495C>T
NM_006418.4:c.1121C>T
NC_000013.11:g.53050359C>T
NC_000013.10:g.53624494C>T
NM_006418.3:c.1121C>T
NP_006409.3:p.Ser374Leu
Position
Human AssemblyChrPosition (strand)Source
GRCh381353,050,359 - 53,050,359CLINVAR
GRCh371353,624,494 - 53,624,494CLINVAR
Build 361352,522,495 - 52,522,495CLINVAR
Cytogenetic Map1313q14.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8627464
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.