Variant #0000262733 (NC_000009.11:g.32989852C>T, NM_175073.2:c.38G>A (APTX))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32989852C>T
DNA change (hg38) g.32989854C>T
Published as APTX(NM_001195249.1):c.38G>A (p.R13Q)
ISCN -
DB-ID APTX_000066
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +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.80G>A r.(?) p.(Arg27Gln)
APTX NM_175073.2 -?/. - c.38G>A r.(?) p.(Arg13Gln)


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