Variant #0001064126 (NC_000003.11:g.183899838G>A, NC_000003.11(NM_004068.3):c.963+3G>A (AP2M1))

Chromosome 3
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.183899838G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ABCF3_000005
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP2M1 NM_004068.3 -?/. - c.963+3G>A r.spl? p.?
ABCF3 NM_018358.2 -?/. - c.-4158G>A r.(?) p.(=)


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