Variant #0000016603 (NC_000016.9:g.53720397_53720400del, NM_015272.2:c.723_726del (RPGRIP1L))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.53720397_53720400del |
| DNA change (hg38) |
g.53686485_53686488del |
| Published as |
c.721-4delAATG: p.N241fsX25 |
| ISCN |
- |
| DB-ID |
RPGRIP1L_000008 |
| Variant remarks |
1 English MKS5 family (com-het) |
| Reference |
PubMed: Otto 2011 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| 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 |
2020-07-09 16:29:39 +02:00 (CEST) |

Variant on transcripts
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