Variant #0000786251 (NC_000003.11:g.?, NM_000187.3:c.1188+2269_1189-2270[TG[n]TA[n] (HGD))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.? |
DNA change (hg38) |
- |
Published as |
HGO-2, D3S4497 |
ISCN |
- |
DB-ID |
HGD_000124 |
Variant remarks |
- |
Reference |
Granadino (1997) - data and classification copied from HGD mutations database |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2021-05-21 10:09:09 +02:00 (CEST) |
Date last edited |
N/A |
Variant on transcripts
|