Variant #0000881391 (NC_000017.10:g.17118555_17118556del, NM_144997.5:c.1379_1380del (FLCN))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.17118555_17118556del
DNA change (hg38) -
Published as -
ISCN -
DB-ID FLCN_000039 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1064793128
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 2022-10-21 08:00:02 +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     
FLCN NM_144997.5 +/. - c.1379_1380del r.(?) p.(Leu460GlnfsTer25)


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