Variant #0000801780 (NC_000005.9:g.112151320A>G, NC_000005.9(NM_000038.5):c.933+30A>G (APC))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.112151320A>G |
DNA change (hg38) |
- |
Published as |
APC(NM_000038.4):c.933+30A>G, APC(NM_000038.6):c.933+30A>G, APC(NM_001127510.1):c.933+30A>G |
ISCN |
- |
DB-ID |
APC_000773 See all 7 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00366 View details |
Owner |
VKGL-NL_NKI |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_NKI |
Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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