Variant #0000569947 (NC_000020.10:g.49510421_49510425del, NM_015339.2:c.831_835del (ADNP))

Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49510421_49510425del
DNA change (hg38) g.50893884_50893888del
Published as ADNP(NM_001282531.2):c.831_835delCAAGA (p.D277Efs*35)
ISCN -
DB-ID ADNP_000084
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 18:14:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADNP NM_015339.2 +/. - c.831_835del r.(?) p.(Asp277GlufsTer35)


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