Variant #0000235367 (NC_000006.11:g.99374786T>C, NM_012160.4:c.79A>G (FBXL4))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.99374786T>C
DNA change (hg38) g.98926910T>C
Published as -
ISCN -
DB-ID FBXL4_000328
Variant remarks -
Reference PubMed: El-Hattab 2017, Journal: El-Hattab 2017
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00039 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-12-04 18:01:33 +01:00 (CET)
Date last edited 2019-02-27 22:42:34 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBXL4 NM_012160.4 ?/. 3 c.79A>G r.(?) p.(Thr27Ala)


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