Variant #0000546774 (NC_000012.11:g.116457069C>T, NM_015335.4:c.969G>A (MED13L))

Chromosome 12
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.116457069C>T
DNA change (hg38) g.116019264C>T
Published as MED13L(NM_015335.4):c.969G>A (p.(Met323Ile)), MED13L(NM_015335.5):c.969G>A (p.M323I)
ISCN -
DB-ID MED13L_000038 See all 2 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) 0.00012 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MED13L NM_015335.4 -?/. - c.969G>A r.(?) p.(Met323Ile)


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