Variant #0001022242 (NC_000023.10:g.129270665C>T, NM_004208.3:c.1117G>A (AIFM1))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.129270665C>T
DNA change (hg38) g.130136690C>T
Published as -
ISCN -
DB-ID AIFM1_000039 See all 3 reported entries
Variant remarks in vitro analysis 293T cells mini-gene exon trapping assay: effect on RNA inclusion of intron sequences
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Tjakko van Ham
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-11-05 16:15:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIFM1 NM_004208.3 +?/. 11 c.1117G>A r.1076_1164del p.Glu359GlyfsTer4


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