chr11:17409631:G>C Detail (hg19) (KCNJ11)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:17,409,631-17,409,631 |
hg38 | chr11:17,388,084-17,388,084 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000525.3:c.8C>G | NP_000516.3:p.Ser3Cys |
NM_001166290.1:c.-16-238C>G | ||
Ensemble | ENST00000339994.5:c.8C>G | ENST00000339994.5:p.Ser3Cys |
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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2013-02-08 | criteria provided, single submitter |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.120 | Neonatal insulin-dependent diabetes mellitus | NA | CLINVAR | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000525.4(KCNJ11):c.8C>G (p.Ser3Cys) AND Neonatal insulin-dependent diabetes mellitus | 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
- rs587783674 dbSNP
- Genome
- hg19
- Position
- chr11:17,409,631-17,409,631
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- C
Genome browser