Variant #0000172019 (NC_000012.11:g.108958089G>A, ISCU(NM_014301.3):c.74G>A)
Chromosome |
12 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.108958089G>A |
DNA change (hg38) |
g.108564313G>A |
Published as |
149G>A (Gly50Glu) |
ISCN |
- |
DB-ID |
ISCU_000002 |
Variant remarks |
- |
Reference |
{PMID9:Kollberg 2009:1956769}, OMIM:var0002 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2010-11-14 16:47:50 +01:00 (CET) |
Date last edited |
2017-06-28 22:52:41 +02:00 (CEST) |

Variant on transcripts
|
|