Variant #0000419216 (NC_000001.10:g.45798561_45798573del, NC_000001.10(NM_001128425.1):c.504+19_504+31del (MUTYH))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45798561_45798573del
DNA change (hg38) g.45332889_45332901del
Published as 462+19_462+31del13
ISCN -
DB-ID MUTYH_000091 See all 11 reported entries
Variant remarks -
Reference Molecular Diagnostics, NSCR Demokritos, Athens, GR
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 13:36:57 +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 +/. 6i c.504+19_504+31del r.[=, 463_504del] p.([=, Lys155_Glu168del]) -



Screenings

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