Variant #0000472756 (NC_000018.9:g.58040022_58040023del, NM_005912.2:c.-439_-438del (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.58040022_58040023del
DNA change (hg38) g.60372789_60372790del
Published as -
ISCN -
DB-ID MC4R_000004 See all 4 reported entries
Variant remarks -
Reference PubMed: Valli-Jaakola et al 2006
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 2020-07-15 08:56:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MC4R NM_005912.2 ?/? ? c.-439_-438del - p.(=)


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