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rs1950952

From SNPedia

Orientationplus
Stabilizedplus
Make rs1950952(C;C)
Make rs1950952(C;G)
Make rs1950952(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position39308472
GeneCTAGE5
is asnp
is mentioned by
dbSNPrs1950952
ebirs1950952
HLIrs1950952
Exacrs1950952
Varsomers1950952
Maprs1950952
PheGenIrs1950952
hapmaprs1950952
1000 genomesrs1950952
hgdprs1950952
ensemblrs1950952
gopubmedrs1950952
geneviewrs1950952
scholarrs1950952
googlers1950952
pharmgkbrs1950952
gwascentralrs1950952
openSNPrs1950952
23andMers1950952
23andMe allrs1950952
SNP Nexus

SNPshotrs1950952
SNPdbers1950952
MSV3drs1950952
GWAS Ctlgrs1950952
GMAF0.4605
Max Magnitude
? (C;C) (C;G) (G;G) 28


Venter snp
Source plos
Gene CTAGE5
allele C
frequency 0.325
sift TOLERATED
HuRef 1103649039317
Disease Association Autoantigen found several cancer, including benign meningioma and cutaneous T-cell lymphoma (CTCL). Isoform 5A and isoform 5B are recognized by patients'sera with tumor specimen of various origins.


GET Evidence
CTAGE5-E360Q
aa_change Glu360Gln
aa_change_short E360Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.600859
summary