Variant #0000058640 (NC_000004.11:g.111539799T>C, NM_153426.2:c.436A>G (PITX2))
| Chromosome |
4 |
| 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.111539799T>C |
| DNA change (hg38) |
g.110618643T>C |
| Published as |
NM_000325.5:c.457A>G (N153D) |
| ISCN |
- |
| DB-ID |
PITX2_000030 See all 2 reported entries |
| Variant remarks |
N153D expression cloning CHO cells reduced activation (0.4) atrial natriuretic factor promoter |
| Reference |
PubMed: Wang 2013, Journal: Wang 2013 |
| 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 |
2015-02-20 21:58:45 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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