Variant #0000807545 (NC_000016.9:g.68856088C>T, NM_004360.3:c.1896C>T (CDH1))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.68856088C>T |
DNA change (hg38) |
- |
Published as |
CDH1(NM_004360.3):c.1896C>T (p.H632=), CDH1(NM_004360.5):c.1896C>T (p.H632=) |
ISCN |
- |
DB-ID |
CDH1_000089 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) |
0.01038 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 |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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