Variant #0000368020 (NC_000001.10:g.45802143C>G, NC_000001.10(NM_001128425.1):c.37-1960G>C (MUTYH))

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.45802143C>G
DNA change (hg38) g.45336471C>G
Published as IVS1+3427 C/G (beta transcript); NM_001048174.1: -6-1960G>C (beta transcript)
ISCN -
DB-ID MUTYH_000165 See all 2 reported entries
Variant remarks -
Reference DUPLICATE – to be removed
ClinVar ID -
dbSNP ID rs3219479
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner InSiGHT - John-Paul Plazzer
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-04-06 17:05:13 +02:00 (CEST)
Date last edited 2019-02-22 12:09:43 +01:00 (CET)
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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.37-1960G>C r.(=) p.(=) -


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