Variant #0000414234 (NC_000014.8:g.75515191A>T, NM_001040108.1:c.1168T>A (MLH3))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.75515191A>T
DNA change (hg38) g.75048488A>T
Published as -
ISCN -
DB-ID MLH3_000009 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency N.D.
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00035 View details
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2009-08-17 12:28:00 +02:00 (CEST)
Date last edited 2021-09-09 14:48:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH3 NM_001040108.1 ?/. 2 c.1168T>A r.(?) p.(Phe390Ile)


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