Variant #0000016598 (NC_000016.9:g.53726113T>A, NM_015272.2:c.394A>T (RPGRIP1L))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.53726113T>A |
| DNA change (hg38) |
g.53692201T>A |
| Published as |
R132X |
| ISCN |
- |
| DB-ID |
RPGRIP1L_000013 See all 3 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs121918201 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-12-04 16:00:56 +01:00 (CET) |
| Date last edited |
2023-11-28 16:07:42 +01:00 (CET) |

Variant on transcripts
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