Variant #0000433787 (NC_000003.11:g.37042515A>G, NM_000249.3:c.277A>G (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.37042515A>G
DNA change (hg38) g.37001024A>G
Published as -
ISCN -
DB-ID MLH1_000967 See all 43 reported entries
Variant remarks Authors describe this as non-pathogenic and not to have an association with HNPCC. NOTE: Functional assay was done on the corresponding yeast allele Q90G.
Reference PubMed: Wanat 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Michael Woods
Database submission license No license selected
Created by Michael Woods
Date created 2007-03-06 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 -/. 3 c.277A>G r.(?) p.(Ser93Gly)


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