Variant #0000473565 (NC_000018.9:g.58038722A>Y, NM_005912.2:c.(861T>R) (MC4R))

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.58038722A>Y
DNA change (hg38) -
Published as Y287X
ISCN -
DB-ID MC4R_000000 See all 10 reported entries
Variant remarks Variant Error [EMISMATCH/EUNCERTAIN]: This transcript variant has an error. Please fix this entry and then remove this message.
Reference PubMed: Yeo et al 2003
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Linda van den Berg
Database submission license No license selected
Created by Linda van den Berg
Date created 2010-10-22 15:10:09 +02:00 (CEST)
Date last edited 2011-01-19 13:14:37 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MC4R NM_005912.2 ?/? ? c.(861T>R) r.(?) p.(Tyr287*)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.