Variant #0000414233 (NC_000014.8:g.75515437_75515438insA, NM_001040108.1:c.921_922insT (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.75515437_75515438insA
DNA change (hg38) g.75048734_75048735insA
Published as -
ISCN -
DB-ID MLH3_000008 See all 2 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) 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 2009-08-17 14:15:00 +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.921_922insT r.(?) p.(Ile308Tyrfs*2)


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