Variant #0000132571 (NC_000007.13:g.83634817T>C, NM_006080.2:c.1198A>G (SEMA3A))
| Chromosome |
7 |
| 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.83634817T>C |
| DNA change (hg38) |
g.84005501T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SEMA3A_000009 See all 2 reported entries |
| Variant remarks |
cDNA expression cloning in GN11 cells (embryonic) showed reduced SEMA3A signaling activity and in COS7 cells normal SEMA3A secretion |
| Reference |
PubMed: Hanchate 2012, Journal: Hanchate 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00022 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2016-10-21 16:42:56 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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