Variant #0000565145 (NC_000018.9:g.56008977G>A, NM_001144964.1:c.962G>A (NEDD4L))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56008977G>A
DNA change (hg38) g.58341745G>A
Published as NEDD4L(NM_001144967.3):c.1325G>A (p.R442H)
ISCN -
DB-ID NEDD4L_000009
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) 0.00016 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NEDD4L NM_001144964.1 -?/. - c.962G>A r.(?) p.(Arg321His)
NEDD4L NM_001144967.2 -?/. - c.1325G>A r.(?) p.(Arg442His)


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