Variant #0000891794 (NC_000014.8:g.50101511C>T, NM_001083908.1:c.357G>A (DNAAF2))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.50101511C>T
DNA change (hg38) -
Published as DNAAF2(NM_018139.3):c.357G>A (p.W119*)
ISCN -
DB-ID DNAAF2_000033
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2026-01-20 18:57:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNAAF2 NM_001083908.1 +/. - c.357G>A r.(?) p.(Trp119*)
DNAAF2 NM_018139.2 +/. - c.357G>A r.(?) p.(Trp119*)


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