Variant #0000658048 (NC_000017.10:g.17122362C>G, NM_144997.5:c.1033G>C (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.17122362C>G
DNA change (hg38) g.17219048C>G
Published as FLCN(NM_001353230.1):c.1033G>C (p.V345L)
ISCN -
DB-ID PLD6_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
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.1033G>C r.(?) p.(Val345Leu)
PLD6 NM_178836.3 -?/. - c.-12762G>C r.(?) p.(=)


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