Variant #0000349958 (NC_000001.10:g.45798475T>C, NM_001128425.1:c.536A>G (MUTYH))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45798475T>C
DNA change (hg38) g.45332803T>C
Published as MUTYH(NM_001048171.1):c.494A>G (p.(Tyr165Cys)), MUTYH(NM_001128425.1):c.536A>G (p.Y179C), MUTYH(NM_001128425.2):c.536A>G (p.Y179C)
ISCN -
DB-ID MUTYH_000012 See all 591 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) 0.00149 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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 +/. - c.536A>G r.(?) p.(Tyr179Cys) -
TOE1 NM_025077.3 +/. - c.-7450T>C r.(?) p.(=) -
HPDL NM_032756.2 +/. - c.*4539T>C r.(=) p.(=) -


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