Variant #0000356395 (NC_000003.11:g.37042476T>G, NM_000249.3:c.238T>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.37042476T>G
DNA change (hg38) g.37000985T>G
Published as -
ISCN -
DB-ID MLH1_000150 See all 21 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 2019-11-01 02:04:48 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 +?/+? 3 c.238T>G r.238u>g p.(Phe80Val)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.