Variant #0000086730 (NC_000003.11:g.179137232C>T, NM_021629.3:c.158G>A (GNB4))
| Chromosome |
3 |
| 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.179137232C>T |
| DNA change (hg38) |
g.179419444C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GNB4_000002 See all 2 reported entries |
| Variant remarks |
expression cloning, no effect protein stability, reduced bradykinin-induced PLCbeta2 activation |
| Reference |
PubMed: Soong 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
1/251 families |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2013-03-15 19:39:16 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
Screenings
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