Variant #0000612077 (NC_000009.11:g.32984710A>C, NM_175073.2:c.689T>G (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.32984710A>C
DNA change (hg38) g.32984712A>C
Published as APTX(NM_001195249.1):c.689T>G (p.V230G), APTX(NM_175073.2):c.689T>G (p.V230G)
ISCN -
DB-ID APTX_000013 See all 6 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) 2.0E-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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +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.731T>G r.(?) p.(Val244Gly)
APTX NM_175073.2 ?/. - c.689T>G r.(?) p.(Val230Gly)


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