Variant #0000604951 (NC_000001.10:g.161192879_161192884del, NM_004106.1:c.*4146_*4151del (FCER1G))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.161192879_161192884del
DNA change (hg38) g.161223089_161223094del
Published as APOA2(NM_001643.2):c.53-11_53-6delTGTGTG
ISCN -
DB-ID APOA2_000010
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NR1I3 NM_001077469.2 -/. - c.*6621_*6626del r.(=) p.(=)
APOA2 NM_001643.1 -/. - c.53-11_53-6del r.(=) p.(=)
FCER1G NM_004106.1 -/. - c.*4146_*4151del r.(=) p.(=)
NR1I3 NM_005122.4 -/. - c.*6736_*6741del r.(=) p.(=)
TOMM40L NM_032174.4 -/. - c.-3183_-3178del r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.