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Variant : CV92834 (NM_152236.2(GAS2L1):c.246C>T (p.Ala82=)) Homo sapiens

Symbol: CV92834
Name: NM_152236.2(GAS2L1):c.246C>T (p.Ala82=)
Condition: Malignant melanoma [RCV000072932]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: GAS2L1   RASL10A  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_152236.2:c.246C>T
NG_032959.1:g.6345C>T
NC_000022.11:g.29308351C>T
NC_000022.10:g.29704341C>T
NM_006477.3:c.*368+d4581G>A
NM_152236.1:c.246C>T
NP_689422.1:p.Ala82=
NM_006478.4:c.246C>T
NM_006478.3:c.246C>T
NP_006469.2:p.Ala82=
NC_000022.9:g.28034341C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh382229,308,351 - 29,308,351CLINVAR
GRCh372229,704,341 - 29,704,341CLINVAR
Build 362228,034,341 - 28,034,341CLINVAR
Cytogenetic Map2222q12.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8637608
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.