chr10:5952731:A>C Detail (hg38) (IL15RA)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr10:5,994,694-5,994,694 View the variant detail on this assembly version. |
| hg38 | chr10:5,952,731-5,952,731 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_002189.3:c.*364T>G | |
| NM_001256765.1:c.*364T>G | ||
| NM_001243539.1:c.*364T>G |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.448 | |
| 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 |
|---|---|---|---|---|---|
| 0.019 | breast carcinoma | Multivariate logistic regression found SNPs in genes important for T helper type... | BeFree | 23996684 | Detail |
| <0.001 | Malignant neoplasm of breast | Multivariate logistic regression found SNPs in genes important for T helper type... | BeFree | 23996684 | Detail |
| <0.001 | breast carcinoma | Multivariate logistic regression found SNPs in genes important for T helper type... | BeFree | 23996684 | Detail |
| 0.090 | Malignant neoplasm of breast | Multivariate logistic regression found SNPs in genes important for T helper type... | BeFree | 23996684 | Detail |
| 0.005 | Malignant neoplasm of breast | Multivariate logistic regression found SNPs in genes important for T helper type... | BeFree | 23996684 | Detail |
| <0.001 | breast carcinoma | Multivariate logistic regression found SNPs in genes important for T helper type... | BeFree | 23996684 | Detail |
| <0.001 | Malignant neoplasm of breast | Multivariate logistic regression found SNPs in genes important for T helper type... | BeFree | 23996684 | Detail |
| <0.001 | breast carcinoma | Multivariate logistic regression found SNPs in genes important for T helper type... | BeFree | 23996684 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... | DisGeNET | Detail |
| Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... | DisGeNET | Detail |
| Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... | DisGeNET | Detail |
| Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... | DisGeNET | Detail |
| Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... | DisGeNET | Detail |
| Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... | DisGeNET | Detail |
| Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... | DisGeNET | Detail |
| Multivariate logistic regression found SNPs in genes important for T helper type 1 (Th1) immunity (I... | DisGeNET | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs2296135 dbSNP
- Genome
- hg38
- Position
- chr10:5,952,731-5,952,731
- Variant Type
- snv
- Reference Allele
- A
- 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))
- rs2296135
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.4477
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 7503
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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