Variant #0000623195 (NC_000015.9:g.25616335T>C, NM_000462.3:c.995A>G (UBE3A))
Chromosome |
15 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.25616335T>C |
DNA change (hg38) |
g.25371188T>C |
Published as |
UBE3A(NM_000462.3):c.995A>G (p.(Asn332Ser)), UBE3A(NM_001354543.1):c.926A>G (p.N309S) |
ISCN |
- |
DB-ID |
UBE3A_001085 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) |
2.0E-5 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-06 12:43:26 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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