chr2:165353712:C>T Detail (hg19) (GRB14)

Information

Genome

Assembly Position
hg19 chr2:165,353,712-165,353,712
hg38 chr2:164,497,202-164,497,202 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_001303422.1:c.1294+9G>A
NM_004490.2:c.1294+9G>A
Ensemble ENST00000263915.8:c.1294+9G>A
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:0.394
ToMMo:0.387
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:0.360

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 601524 OMIM
HGNC 4565 HGNC
Ensembl ENSG00000115290 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv9320862 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
0.439 obesity Polymorphisms of the peroxisome proliferator-activated receptor-γ (rs1801282) an... BeFree 25928419 Detail
0.287 Diabetes Mellitus, Non-Insulin-Dependent In a large sample of the Caucasians the rs8192673 of the PGC-1α gene and the rs1... BeFree 25928419 Detail
0.393 Diabetes Mellitus, Non-Insulin-Dependent Polymorphisms of the peroxisome proliferator-activated receptor-γ (rs1801282) an... BeFree 25928419 Detail
0.102 obesity The aim of this study was to clarify whether common single nucleotide polymorphi... BeFree 25928419 Detail
Annotation

Annotations

DescrptionSourceLinks
Polymorphisms of the peroxisome proliferator-activated receptor-γ (rs1801282) and its coactivator-1 ... DisGeNET Detail
In a large sample of the Caucasians the rs8192673 of the PGC-1α gene and the rs1801282 of the PPAR-γ... DisGeNET Detail
Polymorphisms of the peroxisome proliferator-activated receptor-γ (rs1801282) and its coactivator-1 ... DisGeNET Detail
The aim of this study was to clarify whether common single nucleotide polymorphisms (SNPs) of the Pe... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg19
Position
chr2:165,353,712-165,353,712
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Filtering Status (HGVD)
PASS
# of samples (HGVD)
1210
Mean of sample read depth (HGVD)
106.59
Standard deviation of sample read depth (HGVD)
47.92
Number of reference allele (HGVD)
1467
Number of alternative allele (HGVD)
953
Allele Frequency (HGVD)
0.39380165289256197
Gene Symbol (HGVD)
GRB14
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs8192673
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.3867
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
6481
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
East Asian Chromosome Counts (ExAC)
8620
East Asian Allele Counts (ExAC)
3102
East Asian Heterozygous Counts (ExAC)
2000
East Asian Homozygous Counts (ExAC)
551
East Asian Allele Frequency (ExAC)
0.35986078886310907
Chromosome Counts in All Race (ExAC)
121150
Allele Counts in All Race (ExAC)
81353
Heterozygous Counts in All Race (ExAC)
25065
Homozygous Counts in All Race (ExAC)
28144
Allele Frequency in All Race (ExAC)
0.6715063970284771
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