Variant #0000434664 (NC_000003.11:g.37067120T>A, NC_000003.11(NM_000249.3):c.1039-8T>A (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.37067120T>A
DNA change (hg38) g.37025629T>A
Published as -
ISCN -
DB-ID MLH1_000877 See all 41 reported entries
Variant remarks mRNA assay (splicing analysis,2015): partial loss exon 12 ( on patient's mRNA)
Reference PubMed: Tricarico 2017
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.026 View details
Owner Maurizio Genuardi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2018-04-02 19:34:02 +02:00 (CEST)
Date last edited 2020-06-12 16:06:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 ?/. - c.1039-8T>A r.(?) p.(=)


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