Variant #0000452740 (NC_000002.11:g.152573981A>G, NM_001271208.1:c.771T>C (NEB))
Chromosome |
2 |
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.152573981A>G |
DNA change (hg38) |
g.151717467A>G |
Published as |
- |
ISCN |
- |
DB-ID |
NEB_000102 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs4611637 |
Origin |
Germline |
Segregation |
- |
Frequency |
0.27-0.88 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.75553 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2009-08-20 15:51:50 +02:00 (CEST) |
Date last edited |
2020-09-25 17:50:04 +02:00 (CEST) |

Variant on transcripts
|