Variant #0000724677 (NC_000014.8:g.21883113C>G, NM_001170629.1:c.2008G>C (CHD8))

Chromosome 14
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.21883113C>G
DNA change (hg38) g.21414954C>G
Published as -
ISCN -
DB-ID CHD8_000073
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2022-08-11 14:25:59 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHD8 NM_001170629.1 ?/. - c.2008G>C r.(?) p.(Val670Leu)


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