Variant #0000420312 (NC_000001.10:g.45805837C>T, MUTYH(NM_001128425.1):c.36+54G>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.45805837C>T |
DNA change (hg38) |
g.45340165C>T |
Published as |
- |
ISCN |
- |
DB-ID |
MUTYH_000230 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs17838009 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Astrid Out |

Variant on transcripts
|
|