Variant #0001043411 (NC_000020.10:g.49510829_49510831dup, NM_015339.2:c.422_424dup (ADNP))

Chromosome 20
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.49510829_49510831dup
DNA change (hg38) -
Published as ADNP(NM_001282531.3):c.422_424dup (p.(Ser141dup)), ADNP(NM_001282531.3):c.422_424dupGCA (p.S141dup)
ISCN -
DB-ID ADNP_000092 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) 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.422_424dup r.(?) p.(Ser141dup)


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