chr12:68158712:CGAG> Detail (hg38) (IFNG)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr12:68,552,492-68,552,495 |
hg38 | chr12:68,158,712-68,158,715 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000619.2:c.115-456_115-453delCTCG | |
Ensemble | ENST00000229135.4:c.115-456_115-453delCTCG |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
<0.001 | malaria | The TA11CAG haplotype (rs2069705 T/C, rs2430561 A/T, rs3138557 (CA)n, rs2069718 ... | BeFree | 25445652 | Detail |
<0.001 | Leprosy, Multibacillary | However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... | BeFree | 22392581 | Detail |
<0.001 | Leprosy, Multibacillary | However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... | BeFree | 22392581 | Detail |
<0.001 | Leprosy, Paucibacillary | However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... | BeFree | 22392581 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
The TA11CAG haplotype (rs2069705 T/C, rs2430561 A/T, rs3138557 (CA)n, rs2069718 T/C, rs2069727 A/G, ... | DisGeNET | Detail |
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... | DisGeNET | Detail |
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... | DisGeNET | Detail |
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs3138557 dbSNP
- Genome
- hg38
- Position
- chr12:68,158,712-68,158,715
- Variant Type
- snv
- Reference Allele
- CGAG
- Alternative Allele
- -
Genome browser