Variant #0000808540 (NC_000018.9:g.56002758G>A, NM_001144964.1:c.751G>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.56002758G>A
DNA change (hg38) -
Published as NEDD4L(NM_001144967.2):c.1114G>A (p.E372K)
ISCN -
DB-ID NEDD4L_000030
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEDD4L NM_001144964.1 ?/. - c.751G>A r.(?) p.(Glu251Lys)
NEDD4L NM_001144967.2 ?/. - c.1114G>A r.(?) p.(Glu372Lys)


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