Variant #0000264468 (NC_000016.9:g.68719119T>C, NM_001793.4:c.1436T>C (CDH3))
Chromosome |
16 |
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.68719119T>C |
DNA change (hg38) |
g.68685216T>C |
Published as |
CDH3(NM_001317195.1):c.1436T>C (p.L479P, p.(Leu479Pro)), CDH3(NM_001793.6):c.1436T>C (p.L479P) |
ISCN |
- |
DB-ID |
CDH3_000010 See all 4 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) |
0.0014 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
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