Variant #0001017062 (NC_000005.9:g.(?_111420575)_(112116548_?)[2], NM_000038.5:c.(?_-653066)_(593_?)[2] (APC))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_111420575)_(112116548_?)[2] |
| DNA change (hg38) |
g.(?_112084878)_(112780851_?)[2] |
| Published as |
GRCh37/hg19 5q22.1-22.2(chr5:111420575-112116548)x3, dup ex1-16 |
| ISCN |
- |
| DB-ID |
APC_002202 |
| Variant remarks |
ACMG PM2_sup |
| Reference |
PubMed: Yin 2024, Journal: Yin 2024 |
| ClinVar ID |
ClinVar-980178 |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| 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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