Variant #0000434229 (NC_000003.11:g.37081687G>T, NM_000249.3:c.1569G>T (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.37081687G>T
DNA change (hg38) g.37040196G>T
Published as -
ISCN -
DB-ID MLH1_001723 See all 21 reported entries
Variant remarks -
Reference PubMed: Takahashi 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Michael Woods
Database submission license No license selected
Created by Michael Woods
Date created 2007-08-14 12:00:00 +02:00 (CEST)
Date last edited 2019-02-20 13:06:39 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 +?/. 14 c.1569G>T c.1569g>u p.Glu523Asp


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