chr11:17474961:T>C Detail (hg38) (ABCC8)

Information

Genome

Assembly Position
hg19 chr11:17,496,508-17,496,508 View the variant detail on this assembly version.
hg38 chr11:17,474,961-17,474,961

HGVS

Type Transcript Protein
RefSeq NM_001287174.1:c.215A>G NP_001274103.1:p.Asn72Ser
NM_000352.4:c.215A>G NP_000343.2:p.Asn72Ser
Ensemble ENST00000302539.9:c.215A>G ENST00000302539.9:p.Asn72Ser
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Likely pathogenic
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
Pathogenic 2007-08-01 no assertion criteria provided Diabetes mellitus, permanent neonatal 3 germline Detail
Likely pathogenic 2023-04-13 criteria provided, single submitter type 2 diabetes mellitus unknown 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.215A>G (p.Asn72Ser) AND Permanent neonatal diabetes mellitus ClinVar Detail
NM_000352.6(ABCC8):c.215A>G (p.Asn72Ser) AND Diabetes mellitus, permanent neonatal 3 ClinVar Detail
NM_000352.6(ABCC8):c.215A>G (p.Asn72Ser) AND Type 2 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
rs80356634 dbSNP
Genome
hg38
Position
chr11:17,474,961-17,474,961
Variant Type
snv
Reference Allele
T
Alternative Allele
C
Genome browser