Variant #0000612078 (NC_000009.11:g.32986007G>A, NM_175073.2:c.505C>T (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.32986007G>A
DNA change (hg38) g.32986009G>A
Published as APTX(NM_001195248.1):c.547C>T (p.(Gln183Ter))
ISCN -
DB-ID APTX_000099
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +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.547C>T r.(?) p.(Gln183Ter)
APTX NM_175073.2 ?/. - c.505C>T r.(?) p.(Gln169Ter)


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