Variant #0000855949 (NC_000021.8:g.34012083G>A, NM_203446.2:c.3712C>T (SYNJ1))
| Chromosome |
21 |
| 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.34012083G>A |
| DNA change (hg38) |
- |
| Published as |
SYNJ1(NM_203446.2):c.3712C>T (p.P1238S) |
| ISCN |
- |
| DB-ID |
SYNJ1_000076 |
| 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) |
6.0E-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 |
2022-05-09 15:47:41 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
|