Variant #0000433534 (NC_000003.11:g.37035112T>C, NM_000249.3:c.74T>C (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.37035112T>C
DNA change (hg38) g.36993621T>C
Published as -
ISCN -
DB-ID MLH1_000050 See all 17 reported entries
Variant remarks Authors describe this as non-pathogenic and to have an association with HNPCC. NOTE: Functional assay was done on the corresponding yeast allele I22T.
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) 0 View details
Owner Michael Woods
Database submission license No license selected
Created by Michael Woods
Date created 2007-03-07 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 -/. 1 c.74T>C r.(?) p.(Ile25Thr)


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