chr8:27434151:A>G Detail (hg38) (PTK2B)

Information

Genome

Assembly Position
hg19 chr8:27,291,668-27,291,668 View the variant detail on this assembly version.
hg38 chr8:27,434,151-27,434,151

HGVS

Type Transcript Protein
RefSeq NM_004103.4:c.1145+19A>G
NM_173176.2:c.1145+19A>G
NM_173174.2:c.1145+19A>G
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:0.003
ToMMo:0.004
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:0.002

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 601212 OMIM
HGNC 9612 HGNC
Ensembl ENSG00000120899 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv32580505 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg38
Position
chr8:27,434,151-27,434,151
Variant Type
snv
Reference Allele
A
Alternative Allele
G
Filtering Status (HGVD)
PASS
# of samples (HGVD)
837
Mean of sample read depth (HGVD)
41.12
Standard deviation of sample read depth (HGVD)
16.84
Number of reference allele (HGVD)
1669
Number of alternative allele (HGVD)
5
Allele Frequency (HGVD)
0.002986857825567503
Gene Symbol (HGVD)
PTK2B
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))
rs201484400
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.0035
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
58
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
East Asian Chromosome Counts (ExAC)
8654
East Asian Allele Counts (ExAC)
13
East Asian Heterozygous Counts (ExAC)
13
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0015021955165241507
Chromosome Counts in All Race (ExAC)
121332
Allele Counts in All Race (ExAC)
33
Heterozygous Counts in All Race (ExAC)
33
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
2.7198101078033823E-4
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