Variant #0000933941 (NC_000002.11:g.216296559_216296568delinsG, NM_212482.1:c.535_544delinsC (FN1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.216296559_216296568delinsG
DNA change (hg38) -
Published as -
ISCN -
DB-ID FN1_000115
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-10-11 10:51:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FN1 NM_212482.1 +?/. - c.535_544delinsC r.(?) p.(Cys179_Ile182delinsLeu)


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