Variant #0000865097 (NC_000017.10:g.17124804C>T, NC_000017.10(NM_144997.5):c.871+47G>A (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.17124804C>T
DNA change (hg38) -
Published as FLCN(NM_144606.5):c.918G>A (p.(Trp306*)), FLCN(NM_144606.6):c.918G>A (p.W306*), FLCN(NM_144606.7):c.918G>A (p.W306*)
ISCN -
DB-ID FLCN_000161 See all 5 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) 0.00047 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +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.871+47G>A r.(=) p.(=)
PLD6 NM_178836.3 -?/. - c.-15204G>A r.(?) p.(=)


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