chr12:121431404:G>A Detail (hg19) (HNF1A)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr12:121,431,404-121,431,404 |
hg38 | chr12:120,993,601-120,993,601 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000545.6:c.608G>A | NP_000536.5:p.Arg203His |
NM_001306179.1:c.608G>A | NP_001293108.1:p.Arg203His | |
Ensemble | ENST00000541395.5:c.608G>A | ENST00000541395.5:p.Arg203His |
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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2017-08-23 | no assertion criteria provided | Diabetes mellitus type 1 |
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Detail |
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2023-11-10 | criteria provided, multiple submitters, no conflicts | not provided |
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Detail |
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2022-04-10 | reviewed by expert panel | Monogenic diabetes |
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Detail |
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2022-08-02 | criteria provided, single submitter | maturity-onset diabetes of the young type 3 |
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Detail |
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2021-04-07 | criteria provided, multiple submitters, no conflicts | Maturity onset diabetes mellitus in young |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.281 | Diabetes Mellitus, Insulin-Dependent | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000545.8(HNF1A):c.608G>A (p.Arg203His) AND Diabetes mellitus type 1 | ClinVar | Detail |
NM_000545.8(HNF1A):c.608G>A (p.Arg203His) AND not provided | ClinVar | Detail |
NM_000545.8(HNF1A):c.608G>A (p.Arg203His) AND Monogenic diabetes | ClinVar | Detail |
NM_000545.8(HNF1A):c.608G>A (p.Arg203His) AND Maturity-onset diabetes of the young type 3 | ClinVar | Detail |
NM_000545.8(HNF1A):c.608G>A (p.Arg203His) AND Maturity onset diabetes mellitus in young | 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
- rs587780357 dbSNP
- Genome
- hg19
- Position
- chr12:121,431,404-121,431,404
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
Genome browser