Variant #0000853963 (NC_000015.9:g.28259941T>C, NM_000275.2:c.1025A>G (OCA2))
Chromosome |
15 |
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.28259941T>C |
DNA change (hg38) |
- |
Published as |
OCA2(NM_000275.2):c.1025A>G (p.Y342C), OCA2(NM_000275.3):c.1025A>G (p.Y342C) |
ISCN |
- |
DB-ID |
OCA2_000033 See all 7 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) |
0.00022 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2022-05-09 15:47:41 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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