Variant #0000348433 (NC_000001.10:g.45797201G>A, NM_001128425.1:c.1214C>T (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.45797201G>A
DNA change (hg38) g.45331529G>A
Published as MUTYH(NM_001048171.1):c.1172C>T (p.(Pro391Leu)), MUTYH(NM_001128425.1):c.1214C>T (p.P405L), MUTYH(NM_001128425.2):c.1214C>T (p.P405L)
ISCN -
DB-ID MUTYH_000077 See all 51 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) 7.0E-5 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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 +/. - c.1214C>T r.(?) p.(Pro405Leu) -
TOE1 NM_025077.3 +/. - c.-8724G>A r.(?) p.(=) -
HPDL NM_032756.2 +/. - c.*3265G>A r.(=) p.(=) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.