Variant #0001037487 (NC_000009.11:g.32986041_32986057del, NC_000009.11(NM_175073.2):c.484-25_484-9del (APTX))

Chromosome 9
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.32986041_32986057del
DNA change (hg38) -
Published as APTX(NM_001195248.2):c.484-25_484-9del
ISCN -
DB-ID APTX_000114
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     
APTX NM_001195248.1 -?/. - c.526-25_526-9del r.(=) p.(=)
APTX NM_175073.2 -?/. - c.484-25_484-9del r.(=) p.(=)


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