Variant #0000983869 (NC_000020.10:g.57896161C>T, NM_000114.2:c.455C>T (EDN3))

Chromosome 20
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.57896161C>T
DNA change (hg38) -
Published as EDN3(NM_207034.3):c.455C>T (p.(Ser152Leu))
ISCN -
DB-ID EDN3_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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EDN3 NM_000114.2 ?/. - c.455C>T r.(?) p.(Ser152Leu)
EDN3 NM_207034.1 ?/. - c.455C>T r.(?) p.(Ser152Leu)


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