Variant #0000537962 (NC_000009.11:g.32986039_32986040insC, NC_000009.11(NM_175073.2):c.484-12_484-11insG (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.32986039_32986040insC
DNA change (hg38) g.32986041_32986042insC
Published as APTX(NM_001195249.2):c.484-12_484-11insG
ISCN -
DB-ID APTX_000090 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APTX NM_001195248.1 -/. - c.526-12_526-11insG r.(=) p.(=)
APTX NM_175073.2 -/. - c.484-12_484-11insG r.(=) p.(=)


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