chr2:204731005:A>T Detail (hg19) (CTLA4)

Information

Genome

Assembly Position
hg19 chr2:204,731,005-204,731,005
hg38 chr2:203,866,282-203,866,282 

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
Influence of cytotoxic T lymphocyte-associated antigen 4 (CTLA4) common polymorphisms on outcome in ... MMMP Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg19
Position
chr2:204,731,005-204,731,005
Variant Type
snv
Reference Allele
A
Alternative Allele
T
MMMP State (molecule) (MMMP)
polymorphism rs4553808
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