Variant #0000864812 (NC_000016.9:g.46694553T>G, NM_018206.4:c.2222A>C (VPS35))
| Chromosome |
16 |
| 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.46694553T>G |
| DNA change (hg38) |
- |
| Published as |
VPS35(NM_018206.5):c.2222A>C (p.Q741P), VPS35(NM_018206.6):c.2222A>C (p.Q741P) |
| ISCN |
- |
| DB-ID |
VPS35_000007 See all 2 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) |
Retrieve |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2022-05-09 16:01:56 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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