chr11:2594119:T>C Detail (hg19) (KCNQ1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:2,594,119-2,594,119 |
hg38 | chr11:2,572,889-2,572,889 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000218.2:c.824T>C | NP_000209.2:p.Phe275Ser |
NM_181798.1:c.443T>C | NP_861463.1:p.Phe148Ser | |
Ensemble | ENST00000496887.7:c.563T>C | ENST00000496887.7:p.Phe188Ser |
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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no assertion provided | Congenital long QT syndrome |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.417 | long QT syndrome | We previously identified a missense mutation F275S located within the S5 transme... | BeFree | 19167356 | Detail |
0.006 | cardiac event | Excitement, exercises, and stress appear to be the triggers for developing cardi... | BeFree | 12442276 | Detail |
0.007 | cardiac event | Excitement, exercises, and stress appear to be the triggers for developing cardi... | BeFree | 12442276 | Detail |
0.133 | Congenital long QT syndrome | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000218.3(KCNQ1):c.824T>C (p.Phe275Ser) AND Congenital long QT syndrome | ClinVar | Detail |
We previously identified a missense mutation F275S located within the S5 transmembrane domain of the... | DisGeNET | Detail |
Excitement, exercises, and stress appear to be the triggers for developing cardiac events (syncope, ... | DisGeNET | Detail |
Excitement, exercises, and stress appear to be the triggers for developing cardiac events (syncope, ... | 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
- rs199472729 dbSNP
- Genome
- hg19
- Position
- chr11:2,594,119-2,594,119
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- C
Genome browser