Variant #0000865098 (NC_000017.10:g.17125868T>A, NM_144997.5:c.726A>T (FLCN))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17125868T>A
DNA change (hg38) -
Published as FLCN(NM_144606.5):c.726A>T (p.(Thr242=)), FLCN(NM_144997.5):c.726A>T (p.T242=), FLCN(NM_144997.7):c.726A>T (p.T242=)
ISCN -
DB-ID FLCN_000074 See all 6 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) 0.01944 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 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.726A>T r.(?) p.(Thr242=)
PLD6 NM_178836.3 -/. - c.-16268A>T r.(?) p.(=)


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