Variant #0001000383 (NC_000012.11:g.99898250T>C, NM_181861.1:c.*771906T>C (APAF1))

Chromosome 12
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.99898250T>C
DNA change (hg38) -
Published as ANKS1B(NM_152788.4):c.1438+4A>G (p.?)
ISCN -
DB-ID ANKS1B_000014
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKS1B NM_020140.3 ?/. - c.-349980A>G r.(?) p.(=)
FAM71C NM_153364.3 ?/. - c.-143703T>C r.(?) p.(=)
APAF1 NM_181861.1 ?/. - c.*771906T>C r.(=) p.(=)


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