Variant #0000857512 (NC_000001.10:g.45797188_45797189dup, NM_001128425.1:c.1227_1228dup (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.45797188_45797189dup
DNA change (hg38) -
Published as MUTYH(NM_001048171.1):c.1185_1186dup (p.(Glu396Glyfs*43)), MUTYH(NM_001128425.1):c.1227_1228dupGG (p.E410Gfs*43), MUTYH(NM_001128425.2):c.1227_1228...
ISCN -
DB-ID MUTYH_000078 See all 42 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) Retrieve
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 2023-04-16 21:50:28 +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 +/. - c.1227_1228dup r.(?) p.(Glu410GlyfsTer43) -
TOE1 NM_025077.3 +/. - c.-8737_-8736dup r.(?) p.(=) -
HPDL NM_032756.2 +/. - c.*3252_*3253dup r.(=) p.(=) -


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