Variant #0000357691 (NC_000014.8:g.75516082G>C, NM_001040108.1:c.277C>G (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.75516082G>C
DNA change (hg38) g.75049379G>C
Published as -
ISCN -
DB-ID MLH3_000002 See all 2 reported entries
Variant remarks -
Reference copied from InSiGHT database
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-03-09 13:27:44 +01:00 (CET)
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.277C>G r.(?) p.(Arg93Gly)


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