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