Variant #0000250803 (NC_000015.9:g.93482864A>G, NM_001271.3:c.608A>G (CHD2))

Chromosome 15
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.93482864A>G
DNA change (hg38) g.92939634A>G
Published as CHD2(NM_001271.3):c.608A>G (p.K203R, p.(Lys203Arg)), CHD2(NM_001271.4):c.608A>G (p.K203R)
ISCN -
DB-ID CHD2_000024 See all 3 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) 0.00336 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CHD2 NM_001271.3 -?/. - c.608A>G r.(?) p.(Lys203Arg)


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