chr11:17474919:A>G Detail (hg38) (ABCC8)

Information

Genome

Assembly Position
hg19 chr11:17,496,466-17,496,466 View the variant detail on this assembly version.
hg38 chr11:17,474,919-17,474,919

HGVS

Type Transcript Protein
RefSeq NM_001287174.1:c.257T>C NP_001274103.1:p.Val86Ala
NM_000352.4:c.257T>C NP_000343.2:p.Val86Ala
Ensemble ENST00000302539.9:c.257T>C ENST00000302539.9:p.Val86Ala
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Uncertain significance
Review star
Show details
Links
Type Database ID Link
Gene MIM 600509 OMIM
HGNC 59 HGNC
Ensembl ENSG00000006071 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
Uncertain significance 2019-06-24 criteria provided, single submitter not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.484 DIABETES MELLITUS, PERMANENT NEONATAL NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000352.6(ABCC8):c.257T>C (p.Val86Ala) AND Permanent neonatal diabetes mellitus ClinVar Detail
NM_000352.6(ABCC8):c.257T>C (p.Val86Ala) AND not provided 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
rs193929360 dbSNP
Genome
hg38
Position
chr11:17,474,919-17,474,919
Variant Type
snv
Reference Allele
A
Alternative Allele
G
Genome browser