Variant #0000275906 (NC_000013.10:g.78475259T>C, NM_000115.3:c.885A>G (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.78475259T>C
DNA change (hg38) g.77901124T>C
Published as EDNRB(NM_001201397.1):c.1155A>G (p.L385=)
ISCN -
DB-ID EDNRB_000045
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 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 -?/. 5 c.885A>G r.(?) p.(Leu295=)
EDNRB NM_001122659.2 -?/. - c.885A>G r.(?) p.(Leu295=)


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