Variant #0000865731 (NC_000018.9:g.55992363C>T, NM_001144964.1:c.286C>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.55992363C>T
DNA change (hg38) -
Published as NEDD4L(NM_001144967.2):c.649C>T (p.R217W)
ISCN -
DB-ID NEDD4L_000032
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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.286C>T r.(?) p.(Arg96Trp)
NEDD4L NM_001144967.2 ?/. - c.649C>T r.(?) p.(Arg217Trp)


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