Variant #0000808543 (NC_000018.9:g.56056382C>T, NM_001144964.1:c.2250C>T (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.56056382C>T
DNA change (hg38) -
Published as NEDD4L(NM_001144964.1):c.2250C>T (p.N750=), NEDD4L(NM_015277.6):c.2553C>T (p.N851=)
ISCN -
DB-ID NEDD4L_000018 See all 2 reported entries
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) 0.00124 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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.2250C>T r.(?) p.(Asn750=)
NEDD4L NM_001144967.2 -?/. - c.2613C>T r.(?) p.(Asn871=)


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