Variant #0000256236 (NC_000009.11:g.32984657A>T, NM_175073.2:c.742T>A (APTX))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.32984657A>T
DNA change (hg38) g.32984659A>T
Published as APTX(NM_001195248.2):c.742T>A (p.(Leu248Met)), APTX(NM_175073.2):c.742T>A (p.L248M)
ISCN -
DB-ID APTX_000058 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) 0.00136 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 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APTX NM_001195248.1 ?/. - c.784T>A r.(?) p.(Leu262Met)
APTX NM_175073.2 ?/. - c.742T>A r.(?) p.(Leu248Met)


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