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Variant : CV87819 (NM_182546.3(VSTM2A):c.634+3726C>T) Homo sapiens

Symbol: CV87819
Name: NM_182546.3(VSTM2A):c.634+3726C>T
Condition: Malignant melanoma [RCV000067911]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: VSTM2A   VSTM2A-OT1  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000007.14:g.54553896C>T
NC_000007.13:g.54621589C>T
NR_038994.1:c.1-u3074C>T
NM_182546.3:c.634+3726C>T
NM_182546.2:c.634+3726C>T
NC_000007.12:g.54589083C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh38754,553,896 - 54,553,896CLINVAR
GRCh37754,621,589 - 54,621,589CLINVAR
Build 36754,589,083 - 54,589,083CLINVAR
Cytogenetic Map77p11.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8632604
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.