Variant #0000324820 (NC_000016.9:g.67197373G>C, NM_018378.2:c.775G>C (FBXL8))

Chromosome 16
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.67197373G>C
DNA change (hg38) g.67163470G>C
Published as FBXL8(NM_018378.2):c.775G>C (p.(Glu259Gln))
ISCN -
DB-ID FBXL8_000001
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) 0.00132 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRADD NM_003789.3 ?/. - c.-3641C>G r.(?) p.(=)
FBXL8 NM_018378.2 ?/. - c.775G>C r.(?) p.(Glu259Gln)


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