Variant #0000432679 (NC_000003.11:g.37035103G>C, MLH1(NM_000249.3):c.65G>C)

Individual ID 00200966
Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.37035103G>C
DNA change (hg38) g.36993612G>C
Published as -
ISCN -
DB-ID MLH1_001732 See all 21 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00012 View details
Owner Jack Ji
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH1 NM_000249.3 -?/. 1 c.65G>C r.(?) p.Gly22Ala



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000201936 DNA SEQ - screen date 2015-01-01 MLH1, MSH2, MSH6, PMS2 11 Jack Ji