chr14:77326864:G>T Detail (hg38) (GSTZ1)

Information

Genome

Assembly Position
hg19 chr14:77,793,207-77,793,207 View the variant detail on this assembly version.
hg38 chr14:77,326,864-77,326,864

HGVS

Type Transcript Protein
RefSeq NM_001312660.1:c.94G>T NP_001299589.1:p.Glu32Ter
NM_145870.2:c.94G>T NP_665877.1:p.Glu32Ter
NM_145871.2:c.94G>T NP_665878.2:p.Glu32Ter
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
Type Database ID Link
Gene MIM 603758 OMIM
HGNC 4643 HGNC
Ensembl ENSG00000100577 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 Carcinoma of bladder Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... BeFree 22306368 Detail
<0.001 Carcinoma of bladder Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... BeFree 22306368 Detail
<0.001 Malignant neoplasm of urinary bladder Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... BeFree 22306368 Detail
0.003 Malignant neoplasm of urinary bladder Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=... BeFree 22306368 Detail
Annotation

Annotations

DescrptionSourceLinks
Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... DisGeNET Detail
Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... DisGeNET Detail
Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... DisGeNET Detail
Bladder cancer risk overall was associated with GSTO2 Asn142Asp (homozygous; OR=1.4; 95% CI: 1.0-1.9... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs7975 dbSNP
Genome
hg38
Position
chr14:77,326,864-77,326,864
Variant Type
snv
Reference Allele
G
Alternative Allele
T
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