Variant #0000420125 (NC_000001.10:g.45798466C>T, NM_001128425.1:c.545G>A (MUTYH))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45798466C>T |
DNA change (hg38) |
g.45332794C>T |
Published as |
20848659_R154H |
ISCN |
- |
DB-ID |
MUTYH_000041 See all 14 reported entries |
Variant remarks |
in vitro test of the DNA glycosylase activity on adenine mispaired with 8-hydroxyguanine; extremely severely defective |
Reference |
PubMed: Goto 2010 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
Owner |
Carli Tops |
Database submission license |
No license selected |
Created by |
Carli Tops |
Date created |
2010-10-05 19:56:57 +02:00 (CEST) |
Date last edited |
2020-07-14 21:56:45 +02:00 (CEST) |

Variant on transcripts
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