Variant #0000473115 (NC_000018.9:g.(58039247_58039250)insT, NM_005912.2:c.(333_336)insA (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.(58039247_58039250)insT
DNA change (hg38) -
Published as ins A at codon 112
ISCN -
DB-ID MC4R_000000 See all 10 reported entries
Variant remarks Variant Error [ESYNTAX]: This genomic variant has an error (insertion length must be 1). Please fix this entry and then remove this message.
Reference PubMed: Farooqi 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 2011-01-21 13:47:09 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MC4R NM_005912.2 ?/? ? c.(333_336)insA r.(?) p.(?)


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