Variant #0000016587 (NC_000015.9:g.40710457_40710459del, NM_002225.3:c.(1276_1278del) (IVD))
| Chromosome |
15 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.40710457_40710459del |
| DNA change (hg38) |
g.40418258_40418260del |
| Published as |
DEL1 |
| ISCN |
- |
| DB-ID |
IVD_000013 |
| Variant remarks |
Shows residual enzyme activity |
| Reference |
PubMed: Volchenboum et al (2000) |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Ivo F.A.C. Fokkema |
| Database submission license |
Creative Commons Attribution-ShareAlike 4.0 International |
| Created by |
Ivo F.A.C. Fokkema |
| Date created |
2012-11-27 22:52:07 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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