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Variant : CV80154 (NM_176877.2(INADL):c.5231T>G (p.Val1744Gly)) Homo sapiens

Symbol: CV80154
Name: NM_176877.2(INADL):c.5231T>G (p.Val1744Gly)
Condition: Malignant melanoma [RCV000060230]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: PATJ  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NC_000001.9:g.62367165T>G
NM_176877.2:c.5231T>G
NC_000001.11:g.62128905T>G
NC_000001.10:g.62594577T>G
NP_795352.2:p.Val1744Gly
Position
Human AssemblyChrPosition (strand)Source
GRCh38162,128,905 - 62,128,905CLINVAR
GRCh37162,594,577 - 62,594,577CLINVAR
Build 36162,367,165 - 62,367,165CLINVAR
Cytogenetic Map11p31.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8625035
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.