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Variant : CV81879 (NM_001013735.1(FOXB2):c.582C>T (p.Leu194=)) Homo sapiens

Symbol: CV81879
Name: NM_001013735.1(FOXB2):c.582C>T (p.Leu194=)
Condition: Malignant melanoma [RCV000061958]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: FOXB2  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_001013735.1:c.582C>T
NC_000009.12:g.77020236C>T
NC_000009.11:g.79635152C>T
NP_001013757.1:p.Leu194=
NC_000009.10:g.78824972C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh38977,020,236 - 77,020,236CLINVAR
GRCh37979,635,152 - 79,635,152CLINVAR
Build 36978,824,972 - 78,824,972CLINVAR
Cytogenetic Map99q21.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8626735
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.