Variant #0000959506 (NC_000022.10:g.50502546A>G, NM_015166.3:c.976T>C (MLC1))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.50502546A>G
DNA change (hg38) g.50064117A>G
Published as -
ISCN -
DB-ID MLC1_000080 See all 12 reported entries
Variant remarks severe reduction in plasma membrane expression
Reference PubMed: Tejido 2004
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Rogier Min
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-01-26 14:01:44 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLC1 NM_015166.3 +/. - c.976T>C - p.(Cys326Arg)


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