Variant #0000008753 (NC_000014.8:-, MLH3(NM_001040108.1):c.2825C>T)

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MLH3_00002 See all 2 reported entries
Frequency 0.0455
Variant remarks exon01; C2825T; Thr9421Ile
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH3 NM_001040108.1 ./. 02 c.2825C>T - p.Thr942Ile