Variant #0000726974 (NC_000018.9:g.58039473T>A, NM_005912.2:c.110A>T (MC4R))

Chromosome 18
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.58039473T>A
DNA change (hg38) -
Published as MC4R(NM_005912.2):c.110A>T (p.(Asp37Val)), MC4R(NM_005912.3):c.110A>T (p.D37V)
ISCN -
DB-ID MC4R_000018 See all 5 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) 7.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MC4R NM_005912.2 -?/. - c.110A>T r.(?) p.(Asp37Val)


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