Variant #0001075718 (NC_000003.11:g.150911292C>T, NM_001393769.1:c.2089C>T (MED12L))

Chromosome 3
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.150911292C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MED12L_000011
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1358138557
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-29 15:00:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MED12L NM_001393769.1 ?/. - c.2089C>T r.(?) p.(Pro697Ser)


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