Variant #0000509610 (NC_000002.11:g.152536234C>G, NC_000002.11(NM_001271208.1):c.3255+1G>C (NEB))
Chromosome |
2 |
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.152536234C>G |
DNA change (hg38) |
g.151679720C>G |
Published as |
NEB(NM_001164507.1):c.3255+1G>C (p.?) |
ISCN |
- |
DB-ID |
NEB_000069 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 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-06-09 18:30:23 +02:00 (CEST) |

Variant on transcripts
|