Variant #0000678344 (NC_000008.10:g.17726477dup, NM_004467.3:c.545dup (FGL1))

Chromosome 8
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.17726477dup
DNA change (hg38) -
Published as FGL1(NM_004467.4):c.545dup (p.(Asn182Lysfs*2)), FGL1(NM_201553.1):c.545dupA (p.N182Kfs*2)
ISCN -
DB-ID FGL1_000002 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGL1 NM_004467.3 ?/. - c.545dup r.(?) p.(Asn182LysfsTer2)


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