Variant #0000367923 (NC_000001.10:g.45797481C>T, NM_001128425.1:c.1038G>A (MUTYH))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45797481C>T |
| DNA change (hg38) |
g.45331809C>T |
| Published as |
996G>A; G996A (Ser332Ser) |
| ISCN |
- |
| DB-ID |
MUTYH_000064 See all 7 reported entries |
| Variant remarks |
- |
| Reference |
DUPLICATE – to be removed |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
5.0E-5 View details |
| Owner |
InSiGHT - John-Paul Plazzer |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2018-04-06 17:05:13 +02:00 (CEST) |
| Date last edited |
2020-06-04 13:27:43 +02:00 (CEST) |

Variant on transcripts
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