Variant #0000691998 (NC_000016.9:g.21771818T>C, NM_144672.3:c.3377T>C (OTOA))
Chromosome |
16 |
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.21771818T>C |
DNA change (hg38) |
- |
Published as |
OTOA(NM_144672.4):c.3377T>C (p.L1126P) |
ISCN |
- |
DB-ID |
OTOA_000067 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) |
0.00026 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-09-15 15:50:26 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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