Variant #0000420336 (NC_000001.10:g.45803947dup, MUTYH(NM_001128425.1):c.36+1946dup)

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.45803947dup
DNA change (hg38) g.45338275dup
Published as -
ISCN -
DB-ID MUTYH_000296 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs35804643
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Astrid Out
Database submission license No license selected
Created by Astrid Out
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 ?/. 1i c.36+1946dup r.(?) p.(=) -