chr22:20113073:T>A Detail (hg38) (TRMT2A)

Information

Genome

Assembly Position
hg19 chr22:20,100,596-20,100,596 View the variant detail on this assembly version.
hg38 chr22:20,113,073-20,113,073

HGVS

Type Transcript Protein
RefSeq NM_001257994.1:c.1549+45A>T
NM_022727.5:c.1549+45A>T
NM_182984.4:c.1549+45A>T
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:[No Data.]
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 611151 OMIM
HGNC 24974 HGNC
Ensembl ENSG00000099899 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
0.097 schizophrenia For further support from within the Han Chinese ethnic group, we selected two si... BeFree 18075473 Detail
Annotation

Annotations

DescrptionSourceLinks
For further support from within the Han Chinese ethnic group, we selected two single nucleotide poly... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg38
Position
chr22:20,113,073-20,113,073
Variant Type
snv
Reference Allele
T
Alternative Allele
A
East Asian Chromosome Counts (ExAC)
8602
East Asian Allele Counts (ExAC)
0
East Asian Heterozygous Counts (ExAC)
0
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0
Chromosome Counts in All Race (ExAC)
120130
Allele Counts in All Race (ExAC)
2
Heterozygous Counts in All Race (ExAC)
2
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
1.6648630650129026E-5
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