Variant #0001039746 (NC_000013.10:g.78474776G>C, NM_000115.3:c.965C>G (EDNRB))

Chromosome 13
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.78474776G>C
DNA change (hg38) -
Published as EDNRB(NM_001122659.3):c.965C>G (p.(Ala322Gly))
ISCN -
DB-ID EDNRB_000132
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EDNRB NM_000115.3 ?/. - c.965C>G r.(?) p.(Ala322Gly)
EDNRB NM_001122659.2 ?/. - c.965C>G r.(?) p.(Ala322Gly)


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