Variant #0000147739 (NC_000011.9:g.88911696C>A, NM_000372.4:c.575C>A (TYR))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.88911696C>A |
| DNA change (hg38) |
g.89178528C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TYR_000012 See all 165 reported entries |
| Variant remarks |
enzyme assay showed reduced (0.40) tyrosine hydroxylase and DOPA oxidase activities |
| Reference |
PubMed: Chaki 2011, Journal: Chanki 2001 |
| ClinVar ID |
- |
| dbSNP ID |
rs1042602 |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.25452 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2016-12-02 16:59:06 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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