Variant #0000355793 (NC_000003.11:g.37067410G>A, NM_000249.3:c.1321G>A (MLH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method InSiGHT
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.37067410G>A
DNA change (hg38) g.37025919G>A
Published as -
ISCN -
DB-ID MLH1_000446 See all 35 reported entries
Variant remarks Insight class: 1
Reference InSiGHT
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00034 View details
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 -/- 12 c.1321G>A r.(?) p.(Ala441Thr)


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