chr11:17387103:T>C Detail (hg38) (KCNJ11)

Information

Genome

Assembly Position
hg19 chr11:17,408,650-17,408,650 View the variant detail on this assembly version.
hg38 chr11:17,387,103-17,387,103

HGVS

Type Transcript Protein
RefSeq NM_000525.3:c.989A>G NP_000516.3:p.Tyr330Cys
NM_001166290.1:c.728A>G NP_001159762.1:p.Tyr243Cys
Ensemble ENST00000339994.5:c.989A>G ENST00000339994.5:p.Tyr330Cys
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic Likely pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 600937 OMIM
HGNC 6257 HGNC
Ensembl ENSG00000187486 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
not provided no assertion provided permanent neonatal diabetes mellitus unknown Detail
Pathogenic 2013-02-08 criteria provided, single submitter germline Detail
Likely pathogenic criteria provided, single submitter type 2 diabetes mellitus somatic Detail
Pathogenic 2023-06-16 criteria provided, single submitter not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.569 DIABETES MELLITUS, PERMANENT NEONATAL NA CLINVAR Detail
0.120 Neonatal insulin-dependent diabetes mellitus NA CLINVAR Detail
0.569 DIABETES MELLITUS, PERMANENT NEONATAL We tested the functional effects of two Kir6.2 mutations (Y330C, F333I) that cau... BeFree 15962003 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000525.4(KCNJ11):c.989A>G (p.Tyr330Cys) AND Permanent neonatal diabetes mellitus ClinVar Detail
NM_000525.4(KCNJ11):c.989A>G (p.Tyr330Cys) AND Neonatal insulin-dependent diabetes mellitus ClinVar Detail
NM_000525.4(KCNJ11):c.989A>G (p.Tyr330Cys) AND Type 2 diabetes mellitus ClinVar Detail
NM_000525.4(KCNJ11):c.989A>G (p.Tyr330Cys) AND not provided ClinVar Detail
NA DisGeNET Detail
NA DisGeNET Detail
We tested the functional effects of two Kir6.2 mutations (Y330C, F333I) that cause permanent neonata... 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
rs193929356 dbSNP
Genome
hg38
Position
chr11:17,387,103-17,387,103
Variant Type
snv
Reference Allele
T
Alternative Allele
C
Genome browser