Variant #0000570132 (NC_000020.10:g.57899443A>C, NM_000114.2:c.646A>C (EDN3))

Chromosome 20
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.57899443A>C
DNA change (hg38) g.59324388A>C
Published as EDN3(NM_207034.2):c.646A>C (p.M216L)
ISCN -
DB-ID EDN3_000020
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EDN3 NM_000114.2 -?/. 5 c.646A>C r.(?) p.(Met216Leu)
EDN3 NM_207034.1 -?/. - c.646A>C r.(?) p.(Met216Leu)


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