Variant #0000710080 (NC_000001.10:g.21880603T>C, NM_000478.4:c.29T>C (ALPL))
| Chromosome |
1 |
| 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.21880603T>C |
| DNA change (hg38) |
g.21554110T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ALPL_000052 See all 3 reported entries |
| Variant remarks |
cDNA expression cloning varriant and variant+WT in MDCKII cells |
| Reference |
PubMed: del Angel 2020 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2020-12-30 15:27:54 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|