Variant #0000848360 (NC_000001.10:g.161192881_161192884dup, NM_004106.1:c.*4148_*4151dup (FCER1G))

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.161192881_161192884dup
DNA change (hg38) -
Published as APOA2(NM_001643.1):c.53-9_53-6dupTGTG, APOA2(NM_001643.2):c.53-9_53-6dupTGTG
ISCN -
DB-ID APOA2_000013 See all 3 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
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.*6623_*6626dup r.(=) p.(=)
APOA2 NM_001643.1 -?/. - c.53-9_53-6dup r.(=) p.(=)
FCER1G NM_004106.1 -?/. - c.*4148_*4151dup r.(=) p.(=)
NR1I3 NM_005122.4 -?/. - c.*6738_*6741dup r.(=) p.(=)
TOMM40L NM_032174.4 -?/. - c.-3181_-3178dup r.(?) p.(=)


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