Variant #0000418204 (NC_000001.10:g.45800033T>C, NC_000001.10(NM_001128425.1):c.157+30A>G (MUTYH))

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.45800033T>C
DNA change (hg38) g.45334361T>C
Published as -
ISCN -
DB-ID MUTYH_000006 See all 18 reported entries
Variant remarks -
Reference Clinical Genetics, LUMC, Leiden, NL
ClinVar ID -
dbSNP ID rs3219485
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02382 View details
Owner Carli Tops
Database submission license No license selected
Created by Carli Tops
Date created 2007-04-19 14:01:00 +02:00 (CEST)
Date last edited 2020-08-07 13:09:41 +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 ?/. 2i c.157+30A>G r.(=) p.(=) -



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