Variant #0000097054 (NC_000020.10:g.49508756_49508759del, NM_015339.2:c.2496_2499del (ADNP))

Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49508756_49508759del
DNA change (hg38) g.50892219_50892222del
Published as 2496_2499delTAAA
ISCN -
DB-ID ADNP_000004 See all 8 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Elisa Cappuyns
Database submission license No license selected
Created by Elisa Cappuyns
Date created 2016-05-23 15:45:42 +02:00 (CEST)
Date last edited 2024-10-23 12:40:41 +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 ./. 5 c.2496_2499del r.(?) p.(Asn832Lysfs*81)


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