Variant #0000434766 (NC_000009.11:g.?, NM_000550.2:c.? (TYRP1))
| Chromosome |
9 |
| 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.? |
| DNA change (hg38) |
- |
| Published as |
844T>C (Ser243Ser) |
| ISCN |
- |
| DB-ID |
TYRP1_000003 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs35866166 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
William (Bill) Oetting |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
William (Bill) Oetting |
| Date created |
2011-10-18 16:27:13 +02:00 (CEST) |
| Date last edited |
2021-09-09 14:41:03 +02:00 (CEST) |
Variant on transcripts
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