chr21:34809693:C>T Detail (hg19) (IFNGR2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr21:34,809,693-34,809,693 |
hg38 | chr21:33,437,386-33,437,386 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_005534.3:c.*424C>T | |
NM_001329128.1:c.*424C>T | ||
Ensemble | ENST00000290219.11:c.*424C>T |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.811 | |
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
- rs1059293 dbSNP
- Genome
- hg19
- Position
- chr21:34,809,693-34,809,693
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
- 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))
- rs1059293
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.8112
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 13595
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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