Variant #0001080249 (NC_000014.8:g.21899306G>C, NM_001170629.1:c.497C>G (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.21899306G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr14_005809
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2502015324
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-07-17 13:46:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHD8 NM_001170629.1 ?/. - c.497C>G r.(?) p.(Pro166Arg)


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