Variant #0000262734 (NC_000009.11:g.32987568T>C, NM_175073.2:c.457A>G (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.32987568T>C
DNA change (hg38) g.32987570T>C
Published as APTX(NM_001195249.1):c.457A>G (p.K153E)
ISCN -
DB-ID APTX_000078
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) 0.00082 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.499A>G r.(?) p.(Lys167Glu)
APTX NM_175073.2 -/. - c.457A>G r.(?) p.(Lys153Glu)


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