Variant #0000338770 (NC_000013.10:g.78472470C>T, NC_000013.10(NM_000115.3):c.1195-1G>A (EDNRB))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78472470C>T
DNA change (hg38) g.77898335C>T
Published as -
ISCN -
DB-ID EDNRB_000053
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +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 +/. 7i c.1195-1G>A r.spl? p.?
EDNRB NM_001122659.2 +/. - c.1195-1G>A r.spl? p.?


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