Variant #0000860476 (NC_000006.11:g.65098735T>C, NC_000006.11(NM_001142800.1):c.5928-2A>G (EYS))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.65098735T>C |
| DNA change (hg38) |
- |
| Published as |
EYS(NM_001142800.2):c.5928-2A>G, EYS(NM_001292009.1):c.5928-2A>G, EYS(NM_001292009.2):c.5928-2A>G |
| ISCN |
- |
| DB-ID |
EYS_000158 See all 23 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) |
3.0E-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 |
2022-05-09 15:51:19 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|