Variant #0000560449 (NC_000017.10:g.17119716dup, NM_144997.5:c.1285dup (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.17119716dup
DNA change (hg38) g.17216402dup
Published as FLCN(NM_144997.7):c.1285dupC (p.H429Pfs*27)
ISCN -
DB-ID FLCN_000031 See all 137 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
FLCN NM_144997.5 +/. - c.1285dup r.(?) p.(His429ProfsTer27)
PLD6 NM_178836.3 +/. - c.-10109dup r.(?) p.(=)


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