Variant #0000657910 (NC_000016.9:g.68771362_68771364del, CDH1(NM_004360.3):c.44_46del)
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.68771362_68771364del |
DNA change (hg38) |
g.68737459_68737461del |
Published as |
CDH1(NM_004360.3):c.44_46delTGC (p.L15del) |
ISCN |
- |
DB-ID |
CDH1_000378 |
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) |
Variant not found in online data sets |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |

Variant on transcripts
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