Variant #0000287558 (NC_000017.10:g.17119761C>T, NM_144997.5:c.1233G>A (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.17119761C>T
DNA change (hg38) g.17216447C>T
Published as FLCN(NM_144997.5):c.1233G>A (p.E411=), FLCN(NM_144997.7):c.1233G>A (p.E411=)
ISCN -
DB-ID FLCN_000156 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) 0.01017 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.1233G>A r.(?) p.(Glu411=)
PLD6 NM_178836.3 -/. - c.-10161G>A r.(?) p.(=)


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