Variant #0000841939 (NC_000006.11:g.131900421_131900422delinsGG, NM_000045.3:c.301_302delinsGG (ARG1))
| Chromosome |
6 |
| 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.131900421_131900422delinsGG |
| DNA change (hg38) |
- |
| Published as |
H101G |
| ISCN |
- |
| DB-ID |
ARG1_000093 |
| Variant remarks |
cDNA expression cloning E.coli arginase activity <0.01 |
| Reference |
PubMed: Vockley 1996 |
| 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 |
2022-03-03 20:00:51 +01:00 (CET) |
| Date last edited |
2022-03-06 11:44:23 +01:00 (CET) |

Variant on transcripts
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