Variant #0001017060 (NC_000005.9:g.(?_112112293)_(112251318_?)[2], NM_000038.5:c.(?_531+859)_(*71495_?)[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.(?_112112293)_(112251318_?)[2] |
DNA change (hg38) |
g.(?_112776596)_(112915621_?)[2] |
Published as |
GRCh37/hg19 5q22.2(chr5:112112293-112251318)x3, dup ex1-16 |
ISCN |
- |
DB-ID |
APC_002200 |
Variant remarks |
ACMG PM2_sup |
Reference |
PubMed: Yin 2024, Journal: Yin 2024 |
ClinVar ID |
ClinVar-1341140 |
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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