Variant #0000836763 (NC_000011.9:g.93913262G>C, NM_015368.3:c.1040G>C (PANX1))
| Chromosome |
11 |
| Allele |
Paternal (confirmed) |
| 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.93913262G>C |
| DNA change (hg38) |
g.94180096G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PANX1_000010 See all 2 reported entries |
| Variant remarks |
in vitro expression PANX1 showed altered glycosylation (reduced GLY1, absent GLY2) |
| Reference |
PubMed: Sang 2019 |
| 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 |
2022-01-31 09:12:52 +01:00 (CET) |
| Date last edited |
2022-01-31 09:18:24 +01:00 (CET) |

Variant on transcripts
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