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Variant : CV86986 (NM_001527.3(HDAC2):c.1225C>T (p.Arg409Ter)) Homo sapiens

Symbol: CV86986
Name: NM_001527.3(HDAC2):c.1225C>T (p.Arg409Ter)
Condition: Malignant melanoma [RCV000067077]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: HDAC2  
Variant Type: single nucleotide variant (SO:0001587)
Source: CLINVAR
Molecular Consequence: stop-gain|nonsense|non-coding transcript variant
Evidence: literature only|not provided
HGVS Name(s): NM_001527.3:c.1225C>T
NC_000006.12:g.113943504G>A
NC_000006.11:g.114264668G>A
NR_033441.1:c.1540C>T
NM_001527.2:c.1507C>T
NP_001518.3:p.Arg409Ter
NR_033441.1:n.1540C>T
NC_000006.10:g.114371361G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh386113,943,504 - 113,943,504CLINVAR
GRCh376114,264,668 - 114,264,668CLINVAR
Build 366114,371,361 - 114,371,361CLINVAR
Cytogenetic Map66q21CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8631780
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.