Variant #0000675551 (NC_000001.10:g.181767498G>A, NM_000721.3:c.6341G>A (CACNA1E))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.181767498G>A |
DNA change (hg38) |
- |
Published as |
CACNA1E(NM_000721.4):c.6341G>A (p.R2114Q), CACNA1E(NM_001205293.2):c.6470G>A (p.R2157Q) |
ISCN |
- |
DB-ID |
CACNA1E_000037 See all 2 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) |
0.00046 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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