Variant #0000983868 (NC_000020.10:g.57896160T>C, NM_000114.2:c.454T>C (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.57896160T>C
DNA change (hg38) -
Published as EDN3(NM_207034.3):c.454T>C (p.(Ser152Pro))
ISCN -
DB-ID EDN3_000033
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.454T>C r.(?) p.(Ser152Pro)
EDN3 NM_207034.1 ?/. - c.454T>C r.(?) p.(Ser152Pro)


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