Variant #0001067012 (NC_000018.9:g.55996301G>T, NM_001144964.1:c.392G>T (NEDD4L))

Chromosome 18
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.55996301G>T
DNA change (hg38) -
Published as NEDD4L(NM_001144967.3):c.755G>T (p.(Arg252Leu))
ISCN -
DB-ID NEDD4L_000054
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEDD4L NM_001144964.1 ?/. - c.392G>T r.(?) p.(Arg131Leu)
NEDD4L NM_001144967.2 ?/. - c.755G>T r.(?) p.(Arg252Leu)


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