Variant #0000950805 (NC_000017.10:g.17125875G>A, NM_144997.5:c.719C>T (FLCN))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.17125875G>A
DNA change (hg38) -
Published as FLCN(NM_144997.7):c.719C>T (p.S240L)
ISCN -
DB-ID PLD6_000014
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLCN NM_144997.5 ?/. - c.719C>T r.(?) p.(Ser240Leu)
PLD6 NM_178836.3 ?/. - c.-16275C>T r.(?) p.(=)


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