Variant #0001017091 (NC_000005.9:g.(?_112174106)_(112269758_?)del, NM_000038.5:c.(?_2815)_(*89935_?)del (APC))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_112174106)_(112269758_?)del |
| DNA change (hg38) |
g.(?_112838409)_(112934061_?)del |
| Published as |
GRCh38/hg38 5q22.2(chr5:112838409-112934061)x1, whole gene deletion |
| ISCN |
- |
| DB-ID |
APC_002300 |
| Variant remarks |
ACMG PVS1, PM2_sup |
| Reference |
PubMed: Yin 2024, Journal: Yin 2024 |
| ClinVar ID |
ClinVar-57291 |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Stefan Aretz |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-11-14 12:22:32 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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