chr17:63527220:G>A Detail (hg19) (AXIN2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr17:63,527,220-63,527,220 |
hg38 | chr17:65,531,102-65,531,102 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_004655.3:c.2406-1000C>T | |
Ensemble | ENST00000307078.10:c.2406-1000C>T | |
ENST00000375702.5:c.2211-1000C>T |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.410 | |
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 |
---|---|---|---|---|---|
0.201 | Malignant neoplasm of ovary | We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-cate... | BeFree | 24078348 | Detail |
0.280 | Malignant neoplasm of ovary | We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-cate... | BeFree | 24078348 | Detail |
<0.001 | ovarian carcinoma | We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-cate... | BeFree | 24078348 | Detail |
0.003 | Malignant neoplasm of ovary | We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-cate... | BeFree | 24078348 | Detail |
0.002 | ovarian carcinoma | We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-cate... | BeFree | 24078348 | Detail |
0.082 | ovarian carcinoma | We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-cate... | BeFree | 24078348 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-catenin) [rs4533622, rs2... | DisGeNET | Detail |
We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-catenin) [rs4533622, rs2... | DisGeNET | Detail |
We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-catenin) [rs4533622, rs2... | DisGeNET | Detail |
We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-catenin) [rs4533622, rs2... | DisGeNET | Detail |
We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-catenin) [rs4533622, rs2... | DisGeNET | Detail |
We studied nine single nucleotide polymorphisms (SNPs) located in CTNNB1 (β-catenin) [rs4533622, rs2... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs4074947 dbSNP
- Genome
- hg19
- Position
- chr17:63,527,220-63,527,220
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
- 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))
- rs4074947
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.4104
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 6878
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
Genome browser