Variant #0000414225 (NC_000014.8:g.75516000A>G, NM_001040108.1:c.359T>C (MLH3))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.75516000A>G
DNA change (hg38) g.75049297A>G
Published as -
ISCN -
DB-ID MLH3_000003 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00024 View details
Owner InSiGHT - John-Paul Plazzer
Database submission license No license selected
Created by Rina Kansal
Date created 2014-07-07 21:45:00 +02:00 (CEST)
Date last edited 2019-02-22 10:04:34 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH3 NM_001040108.1 +?/. 2 c.359T>C r.(?) p.(Phe120Ser)


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