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Variant : CV92437 (NM_001039508.1(SIRPG):c.672C>T (p.Val224=)) Homo sapiens

Symbol: CV92437
Name: NM_001039508.1(SIRPG):c.672C>T (p.Val224=)
Condition: Malignant melanoma [RCV000072535]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: SIRPG   SIRPG-AS1  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|synonymous variant|intron variant
Evidence: literature only|not provided
HGVS Name(s): NM_080816.2:c.431-5958C>T
NM_001039508.1:c.672C>T
NM_018556.3:c.672C>T
NC_000020.11:g.1636264G>A
NC_000020.10:g.1616910G>A
XM_001724766.1:c.1-u3496C>T
NP_001034597.1:p.Val224=
NP_061026.2:p.Val224=
NC_000020.9:g.1564910G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38201,636,264 - 1,636,264CLINVAR
GRCh37201,616,910 - 1,616,910CLINVAR
Build 36201,564,910 - 1,564,910CLINVAR
Cytogenetic Map2020p13CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8637211
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.