chr7:128948946:T>C Detail (hg38) (IRF5)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr7:128,589,000-128,589,000 View the variant detail on this assembly version. |
hg38 | chr7:128,948,946-128,948,946 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001098629.2:c.*128T>C | |
NM_001098630.2:c.*128T>C | ||
NM_001098627.3:c.*128T>C |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2007-07-01 | no assertion criteria provided | Systemic lupus erythematosus, association with susceptibility to, 10 |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.004 | Lupus Erythematosus, Discoid | Importantly, our data suggest that in patients with lupus, the presence of the H... | BeFree | 21952918 | Detail |
0.235 | Lupus Erythematosus, Systemic | Importantly, our data suggest that in patients with lupus, the presence of the H... | BeFree | 21952918 | Detail |
0.004 | Lupus Vulgaris | Importantly, our data suggest that in patients with lupus, the presence of the H... | BeFree | 21952918 | Detail |
0.018 | lupus erythematosus | Importantly, our data suggest that in patients with lupus, the presence of the H... | BeFree | 21952918 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_001098629.3(IRF5):c.*128T>C AND Systemic lupus erythematosus, association with susceptibility to,... | ClinVar | Detail |
Importantly, our data suggest that in patients with lupus, the presence of the HLA lupus risk allele... | DisGeNET | Detail |
Importantly, our data suggest that in patients with lupus, the presence of the HLA lupus risk allele... | DisGeNET | Detail |
Importantly, our data suggest that in patients with lupus, the presence of the HLA lupus risk allele... | DisGeNET | Detail |
Importantly, our data suggest that in patients with lupus, the presence of the HLA lupus risk allele... | 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
- rs2070197 dbSNP
- Genome
- hg38
- Position
- chr7:128,948,946-128,948,946
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- C
Genome browser