Variant #0000411435 (NC_000019.9:g.1401397A>G, GAMT(NM_000156.5):c.79T>C)
Chromosome |
19 |
Allele |
Parent #2 |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1401397A>G |
DNA change (hg38) |
g.1401398A>G |
Published as |
- |
ISCN |
- |
DB-ID |
GAMT_012044 See all 5 reported entries |
Variant remarks |
overexpression in primary GAMT deficient fibroblasts restores GAMT activity |
Reference |
Mahmutoglu et al, in preparation |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00277 View details |
Owner |
Gajja Salomons |
Database submission license |
No license selected |
Created by |
Gajja Salomons |

Variant on transcripts
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