Variant #0000418204 (NC_000001.10:g.45800033T>C, NC_000001.10(NM_001128425.1):c.157+30A>G (MUTYH))
Chromosome |
1 |
Allele |
Parent #1 |
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.45800033T>C |
DNA change (hg38) |
g.45334361T>C |
Published as |
- |
ISCN |
- |
DB-ID |
MUTYH_000006 See all 18 reported entries |
Variant remarks |
- |
Reference |
Clinical Genetics, LUMC, Leiden, NL |
ClinVar ID |
- |
dbSNP ID |
rs3219485 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.02382 View details |
Owner |
Carli Tops |
Database submission license |
No license selected |
Created by |
Carli Tops |
Date created |
2007-04-19 14:01:00 +02:00 (CEST) |
Date last edited |
2020-08-07 13:09:41 +02:00 (CEST) |

Variant on transcripts
Screenings
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