Variant #0001000639 (NC_000013.10:g.78492615G>A, NM_000115.3:c.94C>T (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.78492615G>A
DNA change (hg38) -
Published as EDNRB(NM_001201397.1):c.364C>T (p.(Pro122Ser))
ISCN -
DB-ID EDNRB_000129
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) 2.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EDNRB NM_000115.3 -?/. - c.94C>T r.(?) p.(Pro32Ser)
EDNRB NM_001122659.2 -?/. - c.94C>T r.(?) p.(Pro32Ser)


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