Variant #0000046864 (NC_000020.10:g.34810239C>T, NM_012156.2:c.2560C>T (EPB41L1))
| Chromosome |
20 |
| 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.34810239C>T |
| DNA change (hg38) |
g.36222317C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
EPB41L1_000001 See all 2 reported entries |
| Variant remarks |
expression cloning in HEK293 cells shows disruption of 4.1N binding to GluR1 (0.5) by coIP, insertion of AMPAR subunit GluR1 at synaptic membranesignificantly decreased in transfected hippocampal neurons |
| Reference |
PubMed: Hamdan 2011 |
| 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 |
2014-11-14 21:58:23 +01:00 (CET) |
| Date last edited |
2020-07-16 17:10:30 +02:00 (CEST) |

Variant on transcripts
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