Variant #0000420307 (NC_000001.10:g.45806432C>T, MUTYH(NM_001128425.1):c.-216-290G>A)

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.45806432C>T
DNA change (hg38) g.45340760C>T
Published as -
ISCN -
DB-ID MUTYH_000244 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs3219463
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 ?/. _1 c.-216-290G>A r.(?) p.(=) -