Variant #0000951160 (NC_000018.9:g.56063436G>A, NM_001144964.1:c.2500G>A (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.56063436G>A
DNA change (hg38) -
Published as NEDD4L(NM_015277.6):c.2803G>A (p.E935K)
ISCN -
DB-ID NEDD4L_000034
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +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.2500G>A r.(?) p.(Glu834Lys)
NEDD4L NM_001144967.2 ?/. - c.2863G>A r.(?) p.(Glu955Lys)


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