chr21:44287133:G>A Detail (hg38) (AIRE)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr21:45,707,016-45,707,016 View the variant detail on this assembly version. |
hg38 | chr21:44,287,133-44,287,133 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000383.3:c.463G>A | NP_000374.1:p.Gly155Ser |
Ensemble | ENST00000291582.6:c.463G>A | ENST00000291582.6:p.Gly155Ser |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
[No Data.]
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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2023-10-05 | criteria provided, multiple submitters, no conflicts | Polyglandular autoimmune syndrome, type 1 |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.335 | Polyglandular Type I Autoimmune Syndrome | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000383.4(AIRE):c.463G>A (p.Gly155Ser) AND Polyglandular autoimmune syndrome, type 1 | ClinVar | Detail |
NA | 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
- rs193922418 dbSNP
- Genome
- hg38
- Position
- chr21:44,287,133-44,287,133
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
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