chr7:143027881:C>G Detail (hg19) (CLCN1)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr7:143,027,881-143,027,881 |
| hg38 | chr7:143,330,788-143,330,788 View the variant detail on this assembly version. |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000083.2:c.870C>G | NP_000074.2:p.Ile290Met |
| NR_046453.1:c.870C>G | ||
| Ensemble | ENST00000343257.7:c.870C>G | ENST00000343257.7:p.Ile290Met |
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 |
|---|---|---|---|---|---|
Pathogenic
|
1995-08-01 | no assertion criteria provided | Congenital myotonia, autosomal dominant form |
germline
|
Detail |
not provided
|
no assertion provided | Batten-Turner congenital myopathy |
unknown
|
Detail | |
|
Pathogenic
|
2017-01-01 | criteria provided, single submitter |
unknown
|
Detail | |
|
Pathogenic
|
2023-05-05 | criteria provided, single submitter | Congenital myotonia, autosomal dominant form,Congenital myotonia, autosomal recessive form |
germline
|
Detail |
|
Pathogenic
|
2023-05-05 | criteria provided, single submitter | Congenital myotonia, autosomal dominant form,Congenital myotonia, autosomal recessive form |
germline
|
Detail |
|
Pathogenic
|
2020-11-03 | criteria provided, single submitter | not provided |
unknown
|
Detail |
|
Pathogenic
|
2016-01-01 | criteria provided, single submitter | Congenital myotonia, autosomal recessive form |
unknown
|
Detail |
|
Pathogenic
|
2023-08-11 | criteria provided, single submitter | CLCN1-related disorder |
germline
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.495 | Generalized Myotonia of Thomsen | NA | CLINVAR | Detail | |
| 0.388 | myotonia congenita | NA | CLINVAR | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_000083.3(CLCN1):c.870C>G (p.Ile290Met) AND Congenital myotonia, autosomal dominant form | ClinVar | Detail |
| NM_000083.3(CLCN1):c.870C>G (p.Ile290Met) AND Batten-Turner congenital myopathy | ClinVar | Detail |
| NM_000083.3(CLCN1):c.870C>G (p.Ile290Met) AND Myotonia | ClinVar | Detail |
| NM_000083.3(CLCN1):c.870C>G (p.Ile290Met) AND multiple conditions | ClinVar | Detail |
| NM_000083.3(CLCN1):c.870C>G (p.Ile290Met) AND multiple conditions | ClinVar | Detail |
| NM_000083.3(CLCN1):c.870C>G (p.Ile290Met) AND not provided | ClinVar | Detail |
| NM_000083.3(CLCN1):c.870C>G (p.Ile290Met) AND Congenital myotonia, autosomal recessive form | ClinVar | Detail |
| NM_000083.3(CLCN1):c.870C>G (p.Ile290Met) AND CLCN1-related disorder | ClinVar | Detail |
| NA | DisGeNET | 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
- rs80356690 dbSNP
- Genome
- hg19
- Position
- chr7:143,027,881-143,027,881
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- G
Genome browser