Variant #0001050316 (NC_000001.10:g.156561887C>G, NC_000001.10(NM_144772.2):c.183-6C>G (APOA1BP))

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.156561887C>G
DNA change (hg38) -
Published as NAXE(NM_144772.3):c.183-6C>G
ISCN -
DB-ID APOA1BP_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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
TTC24 NM_001105669.2 -?/. - c.*5545C>G r.(=) p.(=)
GPATCH4 NM_015590.3 -?/. - c.*3118G>C r.(=) p.(=)
APOA1BP NM_144772.2 -?/. - c.183-6C>G r.(=) p.(=)


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