Variant #0000258792 (NC_000009.11:g.32986041_32986062del, NC_000009.11(NM_175073.2):c.484-25_484-4del (APTX))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32986041_32986062del
DNA change (hg38) g.32986043_32986064del
Published as APTX(NM_001195249.1):c.484-25_484-4delGTTTTTTTTTTTGTTTTTTTTT, APTX(NM_001195249.2):c.484-25_484-4delGTTTTTTTTTTTGTTTTTTTTT
ISCN -
DB-ID APTX_000071 See all 3 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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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_526-4del r.spl? p.?
APTX NM_175073.2 -/. - c.484-25_484-4del r.spl? p.?


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