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Variant : CV88551 (NM_007234.4(DCTN3):c.208C>T (p.Pro70Ser)) Homo sapiens

Symbol: CV88551
Name: NM_007234.4(DCTN3):c.208C>T (p.Pro70Ser)
Condition: Malignant melanoma [RCV000068644]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: ARID3C   DCTN3  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: literature only|not provided
HGVS Name(s): NC_000009.12:g.34617945G>A
NC_000009.11:g.34617942G>A
NM_001017363.1:c.1239+d3513C>T
NP_009165.1:p.Pro70Ser
NP_077324.1:p.Pro70Ser
NM_007234.4:c.208C>T
NM_024348.3:c.208C>T
NM_007234.3:c.208C>T
NM_024348.2:c.208C>T
NC_000009.10:g.34607942G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38934,617,945 - 34,617,945CLINVAR
GRCh37934,617,942 - 34,617,942CLINVAR
Build 36934,607,942 - 34,607,942CLINVAR
Cytogenetic Map99p13.3CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8633337
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.