Variant #0000863490 (NC_000014.8:g.21853853A>G, NM_001170629.1:c.7665T>C (CHD8))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.21853853A>G
DNA change (hg38) g.21385694A>G
Published as CHD8(NM_001170629.1):c.7665T>C (p.(Asp2555=))
ISCN -
DB-ID CHD8_000079
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) 0.01629 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 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHD8 NM_001170629.1 -?/. - c.7665T>C r.(?) p.(Asp2555=)
SUPT16H NM_007192.3 -?/. - c.-1767T>C r.(?) p.(=)


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