Variant #0000569958 (NC_000020.10:g.49551791_49551792dup, NM_015339.2:c.-4600_-4599dup (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.49551791_49551792dup
DNA change (hg38) g.50935254_50935255dup
Published as DPM1(NM_003859.3):c.679-9_679-8dup
ISCN -
DB-ID DPM1_000007
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DPM1 NM_003859.1 -?/. - c.679-9_679-8dup r.(=) p.(=)
ADNP NM_015339.2 -?/. - c.-4600_-4599dup r.(?) p.(=)


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