Variant #0001039536 (NC_000012.11:g.99548233C>T, NM_181861.1:c.*421889C>T (APAF1))

Chromosome 12
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.99548233C>T
DNA change (hg38) -
Published as ANKS1B(NM_001204068.2):c.38G>A (p.(Arg13His))
ISCN -
DB-ID ANKS1B_000016
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKS1B NM_020140.3 -?/. - c.38G>A r.(?) p.(Arg13His)
FAM71C NM_153364.3 -?/. - c.-493720C>T r.(?) p.(=)
APAF1 NM_181861.1 -?/. - c.*421889C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.