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Variant : CV85381 (NM_138402.4(SP140L):c.1302G>A (p.Val434=)) Homo sapiens

Symbol: CV85381
Name: NM_138402.4(SP140L):c.1302G>A (p.Val434=)
Condition: Malignant melanoma [RCV000065463]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: SP140L  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_138402.4:c.1302G>A
NC_000002.12:g.230400231G>A
NC_000002.11:g.231264946G>A
NP_612411.4:p.Val434=
NC_000002.10:g.230973190G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh382230,400,231 - 230,400,231CLINVAR
GRCh372231,264,946 - 231,264,946CLINVAR
Build 362230,973,190 - 230,973,190CLINVAR
Cytogenetic Map22q37.1CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8630234
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.