Variant #0000551081 (NC_000013.10:g.78475313T>C, NM_000115.3:c.831A>G (EDNRB))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.78475313T>C
DNA change (hg38) g.77901178T>C
Published as EDNRB(NM_001201397.1):c.1101A>G (p.L367=), EDNRB-AS1(NR_103853.1):n.1695-6514T>C
ISCN -
DB-ID EDNRB_000038 See all 2 reported entries
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) 0.57584 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EDNRB NM_000115.3 -/. 5 c.831A>G r.(?) p.(Leu277=)
EDNRB NM_001122659.2 -/. - c.831A>G r.(?) p.(Leu277=)


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