Variant #0001075722 (NC_000003.11:g.151105782A>G, NM_001393769.1:c.5273A>G (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.151105782A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID MED12L_000012
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1163720407
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-29 16:21:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MED12L NM_001393769.1 ?/. - c.5273A>G r.(?) p.(Tyr1758Cys)


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