Variant #0000808545 (NC_000018.9:g.57115306_57115307insA, NM_133459.3:c.683_684insT (CCBE1))
| Chromosome |
18 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.57115306_57115307insA |
| DNA change (hg38) |
- |
| Published as |
CCBE1(NM_133459.3):c.683_684insT (p.(Leu229fs)), CCBE1(NM_133459.4):c.683_684insT (p.L229Pfs*8) |
| ISCN |
- |
| DB-ID |
CCBE1_000014 See all 5 reported entries |
| 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) |
5.0E-5 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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