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Variant : CV84917 (NM_003048.4(SLC9A2):c.1756C>T (p.Arg586Cys)) Homo sapiens

Symbol: CV84917
Name: NM_003048.4(SLC9A2):c.1756C>T (p.Arg586Cys)
Condition: Malignant melanoma [RCV000064999]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: SLC9A2  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NC_000002.12:g.102702413C>T
NC_000002.11:g.103318872C>T
NP_003039.2:p.Arg586Cys
NC_000002.10:g.102685304C>T
NM_003048.4:c.1756C>T
NM_003048.3:c.1756C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh382102,702,413 - 102,702,413CLINVAR
GRCh372103,318,872 - 103,318,872CLINVAR
Build 362102,685,304 - 102,685,304CLINVAR
Cytogenetic Map22q12.1CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8629770
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.