Variant #0000061814 (NC_000003.11:g.128629044_128629046del, NC_000003.11(NM_014049.4):c.1692+52_1692+54del (ACAD9))
| Individual ID |
00034625 |
| Chromosome |
3 |
| Allele |
Parent #1 |
| 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.128629044_128629046del |
| DNA change (hg38) |
g.128910201_128910203del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ACAD9_000008 |
| Variant remarks |
Alamut: UV |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Andreas Laner |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2015-04-02 13:01:39 +02:00 (CEST) |
| Date last edited |
2016-11-12 11:03:31 +01:00 (CET) |

Variant on transcripts
Screenings
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