Variant #0000801346 (NC_000003.11:g.57994496C>T, NM_001457.3:c.205C>T (FLNB))

Chromosome 3
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.57994496C>T
DNA change (hg38) -
Published as FLNB(NM_001457.3):c.205C>T (p.(Arg69Trp)), FLNB(NM_001457.4):c.205C>T (p.R69W)
ISCN -
DB-ID FLNB_000256 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) 4.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
FLNB NM_001457.3 ?/. - c.205C>T r.(?) p.(Arg69Trp) -


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