Variant #0000434162 (NC_000003.11:g.37067306G>A, NM_000249.3:c.1217G>A (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.37067306G>A
DNA change (hg38) g.37025815G>A
Published as -
ISCN -
DB-ID MLH1_000481 See all 64 reported entries
Variant remarks -
Reference PubMed: Kondo 2003
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00088 View details
Owner Michael Woods
Database submission license No license selected
Created by Michael Woods
Date created 2006-04-04 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 ?/. 12 c.1217G>A r.(=) p.(Ser406Asn)


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