Variant #0001017089 (NC_000005.9:g.(?_112043009)_(112179833_?)del, NM_000038.5:c.(?_-30632)_(*10_?)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.(?_112043009)_(112179833_?)del |
DNA change (hg38) |
g.(?_112707312)_(112844136_?)del |
Published as |
whole gene deletion |
ISCN |
- |
DB-ID |
APC_002197 |
Variant remarks |
ACMG PVS1, PM2_sup |
Reference |
PubMed: Yin 2024, Journal: Yin 2024 |
ClinVar ID |
ClinVar-656814 |
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 |
2024-11-14 12:23:24 +01:00 (CET) |

Variant on transcripts
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