Variant #0000655010 (NC_000003.11:g.58148900C>A, NM_001457.3:c.7041C>A (FLNB))

Chromosome 3
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.58148900C>A
DNA change (hg38) g.58163173C>A
Published as FLNB(NM_001164317.1):c.7134C>A (p.F2378L), FLNB(NM_001457.4):c.7041C>A (p.(Phe2347Leu))
ISCN -
DB-ID FLNB_000234 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) 0.00048 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.7041C>A r.(?) p.(Phe2347Leu) -


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