Variant #0000610664 (NC_000007.13:g.128470722G>A, NM_001458.4:c.31G>A (FLNC))

Chromosome 7
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.128470722G>A
DNA change (hg38) g.128830668G>A
Published as FLNC(NM_001458.4):c.31G>A (p.G11S), FLNC(NM_001458.5):c.31G>A (p.G11S)
ISCN -
DB-ID FLNC_000325 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) 7.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
FLNC NM_001458.4 -?/. - c.31G>A r.(?) p.(Gly11Ser) -


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