Variant #0000520712 (NC_000003.11:g.81720076G>A, NM_000158.3:c.342C>T (GBE1))
Chromosome |
3 |
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.81720076G>A |
DNA change (hg38) |
g.81670925G>A |
Published as |
GBE1(NM_000158.3):c.341C>T (p.(=)), GBE1(NM_000158.4):c.342C>T (p.Y114=) |
ISCN |
- |
DB-ID |
GBE1_000029 See all 4 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) |
0.03968 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
|