Variant #0000857514 (NC_000001.10:g.45797846G>A, NM_001128425.1:c.925C>T (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.45797846G>A
DNA change (hg38) -
Published as MUTYH(NM_001048171.1):c.883C>T (p.(Arg295Cys)), MUTYH(NM_001128425.1):c.925C>T (p.R309C), MUTYH(NM_001128425.2):c.925C>T (p.R309C)
ISCN -
DB-ID MUTYH_000019 See all 24 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) 0.00046 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
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.925C>T r.(?) p.(Arg309Cys) -
TOE1 NM_025077.3 ?/. - c.-8079G>A r.(?) p.(=) -
HPDL NM_032756.2 ?/. - c.*3910G>A r.(=) p.(=) -


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