Variant #0000420257 (NC_000001.10:g.45797374del, NM_001128425.1:c.1147del (MUTYH))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45797374del |
DNA change (hg38) |
g.45331702del |
Published as |
15987719_binding_G396D_1147del |
ISCN |
- |
DB-ID |
MUTYH_000069 See all 83 reported entries |
Variant remarks |
DNA binding assay; Patient derived lymphoblastoid cell line; UV A:GO and AO:G binding assay (relatively specific for MUTYH); Reduction in substate binding (similar to reduction in protein expression), 40-50% of WT; residual binding probably from G396D allele |
Reference |
PubMed: Parker 2005 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Astrid Out |
Database submission license |
No license selected |
Created by |
Astrid Out |
Date created |
2010-02-09 11:21:32 +01:00 (CET) |
Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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