Variant #0000537957 (NC_000009.11:g.32974579dup, NC_000009.11(NM_175073.2):c.771-12dup (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.32974579dup
DNA change (hg38) g.32974581dup
Published as APTX(NM_001195249.1):c.771-12dupT, APTX(NM_001195249.2):c.771-12dupT, APTX(NM_175073.2):c.771-12dupT, APTX(NM_175073.3):c.771-12dupT
ISCN -
DB-ID APTX_000033 See all 4 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APTX NM_001195248.1 -/. - c.813-12dup r.(=) p.(=)
APTX NM_175073.2 -/. - c.771-12dup r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.