Variant #0000987516 (NC_000009.11:g.133333899C>T, NM_000050.4:c.286C>T (ASS1))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.133333899C>T |
| DNA change (hg38) |
g.130458512C>T |
| Published as |
P96S |
| ISCN |
- |
| DB-ID |
ASS1_000141 |
| Variant remarks |
cDNA expression cloning shows 0.35 argininosuccinate synthetase enzyme activity |
| Reference |
PubMed: Diez-Fernandez 2016 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-06-03 16:23:50 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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