chr22:38695099:T>C Detail (hg19) (CSNK1E, TPTEP2-CSNK1E)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr22:38,695,099-38,695,099 |
hg38 | chr22:38,299,094-38,299,094 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001894.4:c.737-160A>G | |
NM_152221.2:c.737-160A>G | ||
Ensemble | ENST00000359867.7:c.737-160A>G |
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001289912.1:c.737-160A>G | |
Ensemble | ENST00000400206.7:c.737-160A>G |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.916 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:[No Data.] |
Prediction
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.005 | bipolar disorder | A multi-locus interaction between rs6442925 in the 5' upstream of BHLHB2, rs1534... | BeFree | 18228528 | Detail |
<0.001 | prostate carcinoma | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
0.005 | Malignant neoplasm of prostate | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
0.003 | Malignant neoplasm of prostate | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
<0.001 | prostate carcinoma | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
0.005 | Malignant neoplasm of prostate | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
0.001 | prostate carcinoma | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
<0.001 | prostate carcinoma | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
<0.001 | prostate carcinoma | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
0.006 | Malignant neoplasm of prostate | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
<0.001 | prostate carcinoma | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
0.005 | Malignant neoplasm of prostate | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
0.003 | Malignant neoplasm of prostate | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
0.003 | Malignant neoplasm of prostate | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
0.003 | Malignant neoplasm of prostate | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
<0.001 | prostate carcinoma | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
<0.001 | prostate carcinoma | Our results showed that at least one SNP in nine core circadian genes (rs885747 ... | BeFree | 19934327 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
A multi-locus interaction between rs6442925 in the 5' upstream of BHLHB2, rs1534891 in CSNK1E, and r... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Our results showed that at least one SNP in nine core circadian genes (rs885747 and rs2289591 in PER... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs1534891 dbSNP
- Genome
- hg19
- Position
- chr22:38,695,099-38,695,099
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- C
- 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))
- rs1534891
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.9161
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 15353
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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