Variant #0000433557 (NC_000003.11:g.37035129_37035130delinsTG, NM_000249.3:c.91_92delinsTG (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.37035129_37035130delinsTG
DNA change (hg38) g.36993638_36993639delinsTG
Published as A31C
ISCN -
DB-ID MLH1_000965 See all 12 reported entries
Variant remarks {GR:395}
Reference PubMed: Auclair 2006
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 -/. 1 c.91_92delinsTG r.91_92delinsug p.Ala31Cys


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