Variant #0000543124 (NC_000011.9:g.17415289C>A, NM_000352.3:c.4563G>T (ABCC8))

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.17415289C>A
DNA change (hg38) g.17393742C>A
Published as ABCC8(NM_000352.3):c.4563G>T (p.(Lys1521Asn))
ISCN -
DB-ID ABCC8_000424
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) 0.00032 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 2022-05-09 15:51:19 +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.4563G>T r.(?) p.(Lys1521Asn)
KCNJ11 NM_000525.3 -?/. - c.-5651G>T r.(?) p.(=)


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