Variant #0000933905 (NC_000018.9:g.58039075T>C, NM_005912.2:c.508A>G (MC4R))

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.58039075T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID MC4R_000104 See all 14 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121913560
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-10-09 10:29:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MC4R NM_005912.2 ?/. - c.508A>G r.(?) p.(Ile170Val)


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