Variant #0000551526 (NC_000014.8:g.21853843T>C, NM_001170629.1:c.7675A>G (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.21853843T>C
DNA change (hg38) g.21385684T>C
Published as CHD8(NM_001170629.1):c.7675A>G (p.(Arg2559Gly)), CHD8(NM_001170629.2):c.7675A>G (p.R2559G)
ISCN -
DB-ID CHD8_000020 See all 2 reported entries
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) 6.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +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.7675A>G r.(?) p.(Arg2559Gly)
SUPT16H NM_007192.3 -?/. - c.-1757A>G r.(?) p.(=)


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