Variant #0000355690 (NC_000003.11:g.37067126A>G, NC_000003.11(NM_000249.3):c.1039-2A>G (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method InSiGHT
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.37067126A>G
DNA change (hg38) g.37025635A>G
Published as -
ISCN -
DB-ID MLH1_000443 See all 4 reported entries
Variant remarks Insight class: 4
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 2018-11-09 18:15:18 +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 +?/+? 11i c.1039-2A>G r.1039_1409del p.(Thr347Lysfs*8)


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