Variant #0001036019 (NC_000007.13:g.102665617C>T, NM_145032.3:c.388G>A (FBXL13))

Chromosome 7
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.102665617C>T
DNA change (hg38) -
Published as FBXL13(NM_145032.3):c.388G>A (p.(Ala130Thr))
ISCN -
DB-ID FBXL13_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFE4 NM_001085386.1 -?/. - c.*46805C>T r.(=) p.(=)
LRRC17 NM_005824.2 -?/. - c.*81000C>T r.(=) p.(=)
FBXL13 NM_145032.3 -?/. - c.388G>A r.(?) p.(Ala130Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.