Variant #0001053224 (NC_000009.11:g.32984782G>A, NM_175073.2:c.617C>T (APTX))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.32984782G>A
DNA change (hg38) -
Published as APTX(NM_001195248.2):c.617C>T (p.(Pro206Leu))
ISCN -
DB-ID APTX_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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
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.659C>T r.(?) p.(Pro220Leu)
APTX NM_175073.2 ?/. - c.617C>T r.(?) p.(Pro206Leu)


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