Variant #0001049818 (NC_000017.10:g.17140208_17140226dup, NC_000017.10(NM_144997.5):c.-228+3_-228+21dup (FLCN))

Chromosome 17
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.17140208_17140226dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID FLCN_000333
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs370486376
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 2025-10-31 17:08:01 +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     
FLCN NM_144997.5 -?/. - c.-228+3_-228+21dup r.(?) p.(?)


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