Variant #0000368808 (NC_000002.11:g.47600959G>A, EPCAM(NM_002354.2):c.197G>A)
Individual ID |
00164239 |
Chromosome |
2 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47600959G>A |
DNA change (hg38) |
g.47373820G>A |
Published as |
- |
ISCN |
- |
DB-ID |
EPCAM_000056 |
Variant remarks |
- |
Reference |
Sivagnanam 2008; Schnell 2013 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Mamata Sivagnanam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |

Variant on transcripts
Screenings
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