Variant #0000524562 (NC_000005.9:g.140802855_140802857del, NC_000005.9(NM_018916.3):c.2425-71519_2425-71517del (PCDHGA3))
| Chromosome |
5 |
| 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.140802855_140802857del |
| DNA change (hg38) |
- |
| Published as |
PCDHGA11(NM_018914.2):c.2060_2062del (p.(Ser688del)) |
| ISCN |
- |
| DB-ID |
PCDHGA1_000070 |
| 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 |
2020-03-23 16:13:27 +01:00 (CET) |

Variant on transcripts
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