Variant #0000923301 (NC_000002.11:g.152527706C>A, NM_001271208.1:c.4337G>T (NEB))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.152527706C>A |
DNA change (hg38) |
- |
Published as |
NEB(NM_001271208.2):c.4337G>T (p.G1446V) |
ISCN |
- |
DB-ID |
NEB_000140 See all 3 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_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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