Variant #0001032109 (NC_000001.10:g.47134019_47134021del, NM_022745.4:c.56_58del (ATPAF1))

Chromosome 1
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.47134019_47134021del
DNA change (hg38) -
Published as ATPAF1(NM_022745.5):c.56_58del (p.(Glu19del))
ISCN -
DB-ID ATPAF1_000003
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 2025-05-05 21:14:00 +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     
TEX38 NM_001145474.2 -?/. - c.-3588_-3586del r.(?) p.(=)
ATPAF1 NM_022745.4 -?/. - c.56_58del r.(?) p.(Glu19del)


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