Variant #0000305138 (NC_000005.9:g.140589697_140589700del, NM_018932.3:c.1218_1221del (PCDHB12))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.140589697_140589700del |
| DNA change (hg38) |
g.141210125_141210128del |
| Published as |
PCDHB12(NM_018932.3):c.1218_1221delGAGA (p.E406Dfs*25) |
| ISCN |
- |
| DB-ID |
PCDHB12_000002 |
| 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-06-17 17:15:05 +02:00 (CEST) |

Variant on transcripts
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