Variant #0000862396 (NC_000011.9:g.17409602C>T, NM_000352.3:c.*4936G>A (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.17409602C>T
DNA change (hg38) -
Published as KCNJ11(NM_000525.3):c.37G>A (p.(Val13Met)), KCNJ11(NM_000525.4):c.37G>A (p.V13M)
ISCN -
DB-ID ABCC8_000527 See all 2 reported entries
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) 0.0003 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 -?/. - c.*4936G>A r.(=) p.(=)
KCNJ11 NM_000525.3 -?/. - c.37G>A r.(?) p.(Val13Met)


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