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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