Variant #0000852838 (NC_000011.9:g.17415860T>C, NM_000352.3:c.4498A>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.17415860T>C
DNA change (hg38) -
Published as ABCC8(NM_001351295.2):c.4564A>G (p.S1522G)
ISCN -
DB-ID ABCC8_000534
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:40:45 +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.4498A>G r.(?) p.(Ser1500Gly)
KCNJ11 NM_000525.3 ?/. - c.-6222A>G r.(?) p.(=)


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