Variant #0000368018 (NC_000001.10:g.45806206C>T, MUTYH(NM_001128425.1):c.-216-64G>A)
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.45806206C>T |
DNA change (hg38) |
g.45340534C>T |
Published as |
-280G>A |
ISCN |
- |
DB-ID |
MUTYH_000163 See all 3 reported entries |
Variant remarks |
- |
Reference |
DUPLICATE – to be removed |
ClinVar ID |
- |
dbSNP ID |
rs3219465 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
InSiGHT - John-Paul Plazzer |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |

Variant on transcripts
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