Variant #0000419256 (NC_000001.10:g.45800156C>T, NM_001128425.1:c.64G>A (MUTYH))

Chromosome 1
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.45800156C>T
DNA change (hg38) g.45334484C>T
Published as (Val22Met)
ISCN -
DB-ID MUTYH_000005 See all 79 reported entries
Variant remarks -
Reference Molecular Diagnostics, NSCR Demokritos, Athens, GR
ClinVar ID -
dbSNP ID rs3219484
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.04874 View details
Owner Florentia Fostira
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Carli Tops
Date created 2010-04-05 12:13:05 +02:00 (CEST)
Date last edited 2020-08-07 13:25:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 ?/. 2 c.64G>A r.(64g>a) p.(Val22Met) -



Screenings

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