Variant #0000543115 (NC_000011.9:g.17414565G>A, ABCC8(NM_000352.3):c.4719C>T)

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17414565G>A
DNA change (hg38) g.17393018G>A
Published as ABCC8(NM_000352.3):c.4719C>T (p.(Phe1573=))
ISCN -
DB-ID ABCC8_000415
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 -?/. - c.4719C>T r.(?) p.(Phe1573=)
KCNJ11 NM_000525.3 -?/. - c.-4927C>T r.(?) p.(=)