Variant #0000721228 (NC_000007.13:g.128475624C>T, NM_001458.4:c.597C>T (FLNC))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.128475624C>T
DNA change (hg38) -
Published as FLNC(NM_001127487.1):c.597C>T (p.(Ala199=)), FLNC(NM_001458.4):c.597C>T (p.A199=), FLNC(NM_001458.5):c.597C>T (p.A199=)
ISCN -
DB-ID FLNC_000014 See all 5 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) 0.00188 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.597C>T r.(?) p.(Ala199=) -


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