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Variant : CV84110 (NM_006589.2(FAM189B):c.786T>C (p.Asp262=)) Homo sapiens

Symbol: CV84110
Name: NM_006589.2(FAM189B):c.786T>C (p.Asp262=)
Condition: Malignant melanoma [RCV000064191]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: FAM189B   SCAMP3  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_198264.1:c.498T>C
NM_006589.2:c.786T>C
NC_000001.11:g.155251741A>G
NC_000001.10:g.155221532A>G
NM_005698.2:c.*294+d4238T>C
NM_052837.1:c.*292+d4240T>C
NM_005698.3:c.*294+d4238T>C
NM_052837.2:c.*294+d4238T>C
NP_937995.1:p.Asp166=
NP_006580.2:p.Asp262=
NC_000001.9:g.153488156A>G
Position
Human AssemblyChrPosition (strand)Source
GRCh381155,251,741 - 155,251,741CLINVAR
GRCh371155,221,532 - 155,221,532CLINVAR
Build 361153,488,156 - 153,488,156CLINVAR
Cytogenetic Map11q22CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8628967
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.