Variant #0001014277 (NC_000007.13:g.128470939_128470956dup, NM_001458.4:c.248_265dup (FLNC))

Chromosome 7
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.128470939_128470956dup
DNA change (hg38) -
Published as FLNC(NM_001458.4):c.248_265dupACCGCAAGTTCCATCCGC (p.P88_R89insHRKFHP), FLNC(NM_001458.5):c.248_265dupACCGCAAGTTCCATCCGC (p.P88_R89insHRKFHP)
ISCN -
DB-ID FLNC_000327 See all 4 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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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.248_265dup r.(?) p.(Pro88_Arg89insHisArgLysPheHisPro) -


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