Variant #0000433579 (NC_000003.11:g.37038118C>T, NM_000249.3:c.125C>T (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.37038118C>T
DNA change (hg38) g.36996627C>T
Published as A42V
ISCN -
DB-ID MLH1_000005 See all 3 reported entries
Variant remarks {GR:239}
Reference PubMed: Ellison 2004
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Rolf Sijmons
Database submission license No license selected
Created by Rolf Sijmons
Date created 2009-02-06 12:00:00 +01:00 (CET)
Date last edited 2019-02-20 13:06:39 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 +/. 2 c.125C>T r.(?) p.(Ala42Val)


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