Variant #0000973354 (NC_000001.10:g.154956380dup, NM_025207.4:c.210dup (FLAD1))

Chromosome 1
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.154956380dup
DNA change (hg38) -
Published as FLAD1(NM_025207.5):c.210dup (p.(Gly71ArgfsTer31))
ISCN -
DB-ID CKS1B_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) 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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CKS1B NM_001826.2 ?/. - c.*5127dup r.(?) p.(=)
FLAD1 NM_025207.4 ?/. - c.210dup r.(?) p.(Gly71Argfs*31)


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