chr7:150648731:C>G Detail (hg19) (KCNH2)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr7:150,648,731-150,648,731 |
| hg38 | chr7:150,951,643-150,951,643 View the variant detail on this assembly version. |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000238.3:c.1750G>C | NP_000229.1:p.Gly584Arg |
| NM_172057.2:c.730G>C | NP_742054.1:p.Gly244Arg | |
| Ensemble | ENST00000262186.10:c.1750G>C | ENST00000262186.10:p.Gly584Arg |
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 |
|---|---|---|---|---|---|
not provided
|
no assertion provided | Congenital long QT syndrome |
germline
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.132 | Congenital long QT syndrome | NA | CLINVAR | Detail | |
| 0.361 | long QT syndrome 2 | NA | CLINVAR | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_000238.4(KCNH2):c.1750G>C (p.Gly584Arg) AND Congenital long QT syndrome | 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
- rs199473428 dbSNP
- Genome
- hg19
- Position
- chr7:150,648,731-150,648,731
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- G
Genome browser