chr1:206772036:G>A Detail (hg38) (IL10, IL19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr1:206,945,381-206,945,381 View the variant detail on this assembly version. |
| hg38 | chr1:206,772,036-206,772,036 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000572.2:c.165+235C>T | |
| Ensemble | ENST00000423557.1:c.165+235C>T | |
| ENST00000659065.2:c.48+235C>T |
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | ||
| Ensemble | ENST00000656872.2:c.-149+1206G>A | |
| ENST00000659997.3:c.-149+958G>A |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.014 | |
| 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
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| The results demonstrate that uveitis is associated with three haplotype-tagging SNPs (htSNPs) in the... | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs2222202 dbSNP
- Genome
- hg38
- Position
- chr1:206,772,036-206,772,036
- 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))
- rs2222202
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.0144
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 242
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
Genome browser