Variant #0000870264 (NC_000003.11:g.129251616G>T, NC_000003.11(NM_000539.3):c.936+1G>T (RHO))
| Chromosome |
3 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.129251616G>T |
| DNA change (hg38) |
g.129532773G>T |
| Published as |
RHO IVS4+1 G>T |
| ISCN |
- |
| DB-ID |
RHO_000144 See all 12 reported entries |
| Variant remarks |
homozygous; obsolete nucleotide annotation, new extrapolated from protein and databases |
| Reference |
PubMed: Greenberg 2003 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
LOVD |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Anna Tracewska |
| Date created |
2022-06-17 17:08:24 +02:00 (CEST) |
| Date last edited |
2022-06-17 17:08:39 +02:00 (CEST) |

Variant on transcripts
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