Variant #0000356630 (NC_000003.11:g.37035093A>T, NM_000249.3:c.55A>T (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method InSiGHT
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.37035093A>T
DNA change (hg38) g.36993602A>T
Published as -
ISCN -
DB-ID MLH1_000038 See all 11 reported entries
Variant remarks Insight class: 5
Reference InSiGHT
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-03-05 12:40:48 +01:00 (CET)
Date last edited 2019-11-01 02:51:36 +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.55A>T r.(?) p.(Ile19Phe)


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