Variant #0000928969 (NC_000005.9:g.112102960C>T, NM_000038.5:c.295C>T (APC))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.112102960C>T |
DNA change (hg38) |
- |
Published as |
APC(NM_000038.5):c.295C>T (p.(Arg99Trp)), APC(NM_000038.6):c.295C>T (p.R99W), APC(NM_001127511.1):c.295C>T (p.R99W), APC(NM_001127511.3):c.325C>T ... |
ISCN |
- |
DB-ID |
APC_000420 See all 12 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) |
0.0004 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2023-07-07 10:10:56 +02:00 (CEST) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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