Variant #0000235143 (NC_000006.11:g.99374736C>G, NM_012160.4:c.129G>C (FBXL4))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.99374736C>G |
| DNA change (hg38) |
g.98926860C>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FBXL4_000318 |
| Variant remarks |
- |
| Reference |
PubMed: El-Hattab 2017, Journal: El-Hattab 2017 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-12-04 18:01:33 +01:00 (CET) |
| Date last edited |
2019-02-27 22:42:34 +01:00 (CET) |

Variant on transcripts
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