Variant #0000507688 (NC_000001.10:g.45805880G>A, MUTYH(NM_001128425.1):c.36+11C>T)

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45805880G>A
DNA change (hg38) g.45340208G>A
Published as MUTYH(NM_001128425.1):c.36+11C>T (, p.(=)), TOE1(NM_025077.4):c.-45G>A
ISCN -
DB-ID MUTYH_000003 See all 10 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00333 View details
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 -/. - c.36+11C>T r.(=) p.(=) -
TESK2 NM_007170.2 -/. - c.*4632C>T r.(=) p.(=) -
TOE1 NM_025077.3 -/. - c.-45G>A r.(?) p.(=) -