chr6:32038468:G>A Detail (hg38) (CYP21A2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr6:32,006,245-32,006,245 View the variant detail on this assembly version. |
hg38 | chr6:32,038,468-32,038,468 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | ||
Ensemble | ENST00000435122.3:c.46G>A | ENST00000435122.3:p.Ala16Thr |
ENST00000644719.2:c.46G>A | ENST00000644719.2:p.Ala16Thr |
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 | Chronic active hepatitis | By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusi... | BeFree | 15126570 | Detail |
0.042 | Chronic active hepatitis | By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusi... | BeFree | 15126570 | Detail |
<0.001 | Chronic active hepatitis | By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusi... | BeFree | 15126570 | Detail |
0.303 | Congenital adrenal hyperplasia due to 21 hydroxylase deficiency | Functional analysis of two recurrent amino acid substitutions in the CYP21 gene ... | UNIPROT | 15126570 | Detail |
<0.001 | hypertrichosis | By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusi... | BeFree | 15126570 | Detail |
<0.001 | hypertrichosis | By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusi... | BeFree | 15126570 | Detail |
<0.001 | hypertrichosis | By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusi... | BeFree | 15126570 | Detail |
<0.001 | Chronic active hepatitis | By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusi... | BeFree | 15126570 | Detail |
<0.001 | hypertrichosis | By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusi... | BeFree | 15126570 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusion breakpoint downst... | DisGeNET | Detail |
By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusion breakpoint downst... | DisGeNET | Detail |
By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusion breakpoint downst... | DisGeNET | Detail |
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patient... | DisGeNET | Detail |
By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusion breakpoint downst... | DisGeNET | Detail |
By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusion breakpoint downst... | DisGeNET | Detail |
By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusion breakpoint downst... | DisGeNET | Detail |
By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusion breakpoint downst... | DisGeNET | Detail |
By CYP21 gene analysis, we identified a chimeric CYP21P/CYP21 gene with the fusion breakpoint downst... | 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
- rs63749090 dbSNP
- Genome
- hg38
- Position
- chr6:32,038,468-32,038,468
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
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