Variant #0000503809 (NC_000001.10:g.156563851C>T, NM_144772.2:c.842C>T (APOA1BP))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.156563851C>T
DNA change (hg38) g.156594059C>T
Published as NAXE(NM_144772.2):c.842C>T (p.T281I), NAXE(NM_144772.3):c.842C>T (p.(Thr281Ile))
ISCN -
DB-ID APOA1BP_000005 See all 2 reported entries
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) 0.00051 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPATCH4 NM_015590.3 ?/. - c.*1154G>A r.(=) p.(=)
APOA1BP NM_144772.2 ?/. - c.842C>T r.(?) p.(Thr281Ile)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.