Variant #0000614658 (NC_000013.10:g.49050881_49050885dup, NM_000321.2:c.2565_2569dup (RB1))
| Chromosome |
13 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.49050881_49050885dup |
| DNA change (hg38) |
g.48476745_48476749dup |
| Published as |
RB1(NM_000321.2):c.2564_2565insCGACC (p.(Arg857ProfsTer18)) |
| ISCN |
- |
| DB-ID |
LPAR6_000011 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-07-03 17:12:49 +02:00 (CEST) |

Variant on transcripts
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