Variant #0000433469 (NC_000003.11:g.37035047del, NM_000249.3:c.9del (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.37035047del
DNA change (hg38) g.36993556del
Published as 9delC
ISCN -
DB-ID MLH1_000966 See all 5 reported entries
Variant remarks ICCON data, Royal Prince Alfred/Liverpool, NSW
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
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 InSiGHT - John-Paul Plazzer
Date created 2016-07-07 12:00:00 +02:00 (CEST)
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.9del r.(?) p.(Phe3Leufs*14)


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