Variant #0000533327 (NC_000008.10:g.101719035_101719115del, NC_000008.10(NM_002568.3):c.1447+1_1448-1del (PABPC1))
| Chromosome |
8 |
| Allele |
Unknown |
| 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.101719035_101719115del |
| DNA change (hg38) |
g.100706807_100706887del |
| Published as |
PABPC1(NM_002568.3):c.1447+1_1448-1del (p.?) |
| ISCN |
- |
| DB-ID |
PABPC1_000007 |
| 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 |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-06-24 15:09:15 +02:00 (CEST) |

Variant on transcripts
|