Variant #0000147882 (NC_000011.9:g.88911139G>T, NM_000372.4:c.18G>T (TYR))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.88911139G>T |
| DNA change (hg38) |
g.89177971G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TYR_000289 |
| Variant remarks |
copied from the “Albanism Database” (University of Minnesota) |
| Reference |
Albinism Database |
| ClinVar ID |
- |
| dbSNP ID |
rs76180653 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
William (Bill) Oetting |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2016-12-04 10:04:54 +01:00 (CET) |
| Date last edited |
2024-02-02 03:42:58 +01:00 (CET) |

Variant on transcripts
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