Variant #0000655998 (NC_000008.10:g.134270617G>A, NM_006096.3:c.442C>T (NDRG1))
Chromosome |
8 |
Allele |
Unknown |
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.134270617G>A |
DNA change (hg38) |
g.133258374G>A |
Published as |
NDRG1(NM_001135242.2):c.442C>T (p.R148*) |
ISCN |
- |
DB-ID |
NDRG1_000001 See all 5 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) |
Retrieve |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2020-06-24 15:56:17 +02:00 (CEST) |

Variant on transcripts
|