Variant #0001001114 (NC_000014.8:g.68282559T>A, NM_015346.3:c.122A>T (ZFYVE26))

Chromosome 14
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.68282559T>A
DNA change (hg38) -
Published as ZFYVE26(NM_015346.3):c.122A>T (p.(Glu41Val))
ISCN -
DB-ID RAD51B_000025
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) 3.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD51B NM_002877.5 ?/. - c.-4014T>A r.(?) p.(=)
ZFYVE26 NM_015346.3 ?/. - c.122A>T r.(?) p.(Glu41Val)
RAD51B NM_133509.3 ?/. - c.-4014T>A r.(?) p.(=)


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