Variant #0000418196 (NC_000001.10:g.45805816G>C, MUTYH(NM_001128425.1):c.36+75C>G)

Individual ID 00202617
Chromosome 1
Allele Parent #1
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.45805816G>C
DNA change (hg38) g.45340144G>C
Published as -
ISCN -
DB-ID MUTYH_000020 See all 2 reported entries
Variant remarks -
Reference Clinical Genetics, LUMC, Leiden, NL
ClinVar ID -
dbSNP ID rs3219467
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Carli Tops
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 ?/. 1i c.36+75C>G r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000203648 DNA SEQ - - MUTYH 1 Carli Tops