Variant #0000711820 (NC_000008.10:g.?, NM_006269.1:c.? (RP1))
| Chromosome |
8 |
| Allele |
Parent #1 |
| 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.? |
| DNA change (hg38) |
- |
| Published as |
AF143222:6098A>G (TAT?TGT) Cys2033Tyr |
| ISCN |
- |
| DB-ID |
RP1_000000 See all 58 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Sohocki 2001 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Julia Lopez |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2021-01-14 12:40:33 +01:00 (CET) |
| Date last edited |
N/A |
Variant on transcripts
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