Variant #0000573418 (NC_000023.10:g.128691930A>G, NC_000023.10(NM_000276.3):c.439+3A>G (OCRL))
Chromosome |
X |
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.128691930A>G |
DNA change (hg38) |
g.129557953A>G |
Published as |
OCRL(NM_000276.3):c.439+3A>G (p.?), OCRL(NM_000276.4):c.439+3A>G, OCRL(NM_001318784.1):c.442+3A>G |
ISCN |
- |
DB-ID |
OCRL_000059 See all 6 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) |
0.00237 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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