Variant #0000614682 (NC_000013.10:g.78492461C>T, NM_000115.3:c.248G>A (EDNRB))

Chromosome 13
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.78492461C>T
DNA change (hg38) g.77918326C>T
Published as EDNRB(NM_001201397.1):c.518G>A (p.R173H)
ISCN -
DB-ID EDNRB_000067
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EDNRB NM_000115.3 -?/. 2 c.248G>A r.(?) p.(Arg83His)
EDNRB NM_001122659.2 -?/. - c.248G>A r.(?) p.(Arg83His)


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