Variant #0001043405 (NC_000020.10:g.49509095dup, NM_015339.2:c.2156dup (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.49509095dup
DNA change (hg38) -
Published as ADNP(NM_001282531.2):c.2156dupA (p.Y719*), ADNP(NM_001282531.3):c.2156dup (p.(Tyr719Ter)), ADNP(NM_001282531.3):c.2156dupA (p.Y719*)
ISCN -
DB-ID ADNP_000009 See all 5 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADNP NM_015339.2 +/. - c.2156dup r.(?) p.(Tyr719Ter)


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