Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV87843 (NM_004603.3(STX1A):c.76C>T (p.Arg26Ter)) Homo sapiens

Symbol: CV87843
Name: NM_004603.3(STX1A):c.76C>T (p.Arg26Ter)
Condition: Malignant melanoma [RCV000067935]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: MIR4284   STX1A  
Variant Type: single nucleotide variant (SO:0001587)
Source: CLINVAR
Molecular Consequence: stop-gain|nonsense
Evidence: literature only|not provided
HGVS Name(s): NM_001165903.1:c.76C>T
NM_004603.3:c.76C>T
NG_013360.1:g.15611C>T
NC_000007.14:g.73709077G>A
NC_000007.13:g.73123407G>A
NR_036247.1:c.1-u2240G>A
NM_004603.2:c.76C>T
NP_004594.1:p.Arg26Ter
NP_001159375.1:p.Arg26Ter
NC_000007.12:g.72761343G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38773,709,077 - 73,709,077CLINVAR
GRCh37773,123,407 - 73,123,407CLINVAR
Build 36772,761,343 - 72,761,343CLINVAR
Cytogenetic Map77q11.23CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8632628
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.