Variant #0000978674 (NC_000009.11:g.33001564C>A, NC_000009.11(NM_175073.2):c.-111+1G>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.33001564C>A
DNA change (hg38) -
Published as APTX(NM_001195248.2):c.-5+1G>T, APTX(NM_175073.3):c.-111+1G>T
ISCN -
DB-ID APTX_000109 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) 0.00013 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 2024-04-19 20:27:30 +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.38+1G>T r.spl? p.?
APTX NM_175073.2 ?/. - c.-111+1G>T r.spl? p.?


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