Variant #0000414226 (NC_000014.8:g.75515912A>G, NM_001040108.1:c.447T>C (MLH3))

Chromosome 14
Allele Parent #1
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.75515912A>G
DNA change (hg38) g.75049209A>G
Published as 561T>C (Tyr149Tyr)
ISCN -
DB-ID MLH3_000052 See all 3 reported entries
Variant remarks -
Reference PubMed: Lipkin 2001
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 4/120
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 InSiGHT - John-Paul Plazzer
Date created 2008-09-14 12:07:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MLH3 NM_001040108.1 -?/. 2 c.447T>C r.(?) p.(=)


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