Variant #0000865952 (NC_000019.9:g.17753685G>A, NM_001080421.2:c.2441C>T (UNC13A))
Chromosome |
19 |
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.17753685G>A |
DNA change (hg38) |
- |
Published as |
UNC13A(NM_001080421.2):c.2441C>T (p.(Pro814Leu), p.P814L), UNC13A(NM_001080421.3):c.2441C>T (p.P814L) |
ISCN |
- |
DB-ID |
UNC13A_000014 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_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2022-05-09 16:01:56 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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