Variant #0000016977 (NC_000018.9:g.11752435G>A, NM_001142339.2:c.3G>A (GNAL))
| Chromosome |
18 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.11752435G>A |
| DNA change (hg38) |
g.11752436G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GNAL_000004 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Satya Vemula |
| Database submission license |
No license selected |
| Created by |
Satya Vemula |
| Date created |
2013-01-24 21:24:29 +01:00 (CET) |
| Date last edited |
2020-07-14 16:46:22 +02:00 (CEST) |

Variant on transcripts
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