Variant #0001016814 (NC_000002.11:g.26508414T>G, NM_000183.2:c.1364T>G (HADHB))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.26508414T>G |
| DNA change (hg38) |
g.26285546T>G |
| Published as |
(V422G) |
| ISCN |
- |
| DB-ID |
HADHB_000032 See all 4 reported entries |
| Variant remarks |
cDNA expression cloning no apparent residual enzyme activity |
| Reference |
PubMed: Purevsuren 2009 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-11-12 22:09:34 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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