Variant #0000862398 (NC_000011.9:g.17409628C>T, NM_000352.3:c.*4910G>A (ABCC8))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.17409628C>T
DNA change (hg38) -
Published as KCNJ11(NM_000525.3):c.11G>A (p.(Arg4His))
ISCN -
DB-ID KCNJ11_000101 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) 1.0E-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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 ?/. - c.*4910G>A r.(=) p.(=)
KCNJ11 NM_000525.3 ?/. - c.11G>A r.(?) p.(Arg4His)


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