chr1:154465420:T>C Detail (hg38) (IL6R)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr1:154,437,896-154,437,896 View the variant detail on this assembly version. |
hg38 | chr1:154,465,420-154,465,420 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_181359.2:c.*255T>C | |
NM_000565.3:c.*40T>C | ||
Ensemble | ENST00000344086.8:c.*255T>C |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.807 | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:0.847 |
Prediction
ClinVar
Clinical Significance |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2024-01-24 | criteria provided, single submitter | not specified |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
<0.001 | arteriosclerosis | The AAT haplotype of the IL-6R gene (rs4845617 G/A, rs4845623 A/G, and rs2229238... | BeFree | 21835044 | Detail |
0.127 | Coronary heart disease | A genome-wide association study for coronary artery disease identifies a novel s... | GWASCAT | 22319020 | Detail |
0.003 | coronary artery disease | [We have identified a novel locus in the MHC associated with CAD. MHC genes regu... | GAD | 22319020 | Detail |
<0.001 | atherosclerosis | The AAT haplotype of the IL-6R gene (rs4845617 G/A, rs4845623 A/G, and rs2229238... | BeFree | 21835044 | Detail |
<0.001 | Dyslipidemias | The AAT haplotype of the IL-6R gene (rs4845617 G/A, rs4845623 A/G, and rs2229238... | BeFree | 21835044 | Detail |
0.151 | obesity | Boys who carry the GG genotype of CRP +2147 A/G and the CC genotype of IL-6R rs2... | BeFree | 20856253 | Detail |
0.005 | atherosclerosis | The AAT haplotype of the IL-6R gene (rs4845617 G/A, rs4845623 A/G, and rs2229238... | BeFree | 21835044 | Detail |
0.120 | arteriosclerosis | The AAT haplotype of the IL-6R gene (rs4845617 G/A, rs4845623 A/G, and rs2229238... | BeFree | 21835044 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000565.4(IL6R):c.*40T>C AND not specified | ClinVar | Detail |
The AAT haplotype of the IL-6R gene (rs4845617 G/A, rs4845623 A/G, and rs2229238 C/T) may play an im... | DisGeNET | Detail |
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus ... | DisGeNET | Detail |
[We have identified a novel locus in the MHC associated with CAD. MHC genes regulate inflammation an... | DisGeNET | Detail |
The AAT haplotype of the IL-6R gene (rs4845617 G/A, rs4845623 A/G, and rs2229238 C/T) may play an im... | DisGeNET | Detail |
The AAT haplotype of the IL-6R gene (rs4845617 G/A, rs4845623 A/G, and rs2229238 C/T) may play an im... | DisGeNET | Detail |
Boys who carry the GG genotype of CRP +2147 A/G and the CC genotype of IL-6R rs2229238 C/T have a gr... | DisGeNET | Detail |
The AAT haplotype of the IL-6R gene (rs4845617 G/A, rs4845623 A/G, and rs2229238 C/T) may play an im... | DisGeNET | Detail |
The AAT haplotype of the IL-6R gene (rs4845617 G/A, rs4845623 A/G, and rs2229238 C/T) may play an im... | 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
- -
- Genome
- hg38
- Position
- chr1:154,465,420-154,465,420
- 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))
- rs2229238
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.8066
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 13519
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
- East Asian Chromosome Counts (ExAC)
- 8614
- East Asian Allele Counts (ExAC)
- 7296
- East Asian Heterozygous Counts (ExAC)
- 1098
- East Asian Homozygous Counts (ExAC)
- 3099
- East Asian Allele Frequency (ExAC)
- 0.8469932667750174
- Chromosome Counts in All Race (ExAC)
- 118992
- Allele Counts in All Race (ExAC)
- 94901
- Heterozygous Counts in All Race (ExAC)
- 18927
- Homozygous Counts in All Race (ExAC)
- 37987
- Allele Frequency in All Race (ExAC)
- 0.7975410111604141
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