Variant #0000979484 (NC_000011.9:g.17409499T>C, NM_000352.3:c.*5039A>G (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.17409499T>C
DNA change (hg38) -
Published as KCNJ11(NM_000525.4):c.140A>G (p.(Lys47Arg))
ISCN -
DB-ID ABCC8_000634
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC8 NM_000352.3 ?/. - c.*5039A>G r.(=) p.(=)
KCNJ11 NM_000525.3 ?/. - c.140A>G r.(?) p.(Lys47Arg)


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