Variant #0000695764 (NC_000012.11:g.40619460A>C, NC_000012.11(NM_198578.3):c.237+18A>C (LRRK2))
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.40619460A>C |
| DNA change (hg38) |
g.40225658A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
LRRK2_000044 |
| Variant remarks |
- |
| Reference |
PubMed: Rubio 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
1/27900 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Justin Rubio |
| Database submission license |
No license selected |
| Created by |
Justin Rubio |
| Date created |
2012-04-27 21:16:32 +02:00 (CEST) |
| Date last edited |
2020-10-03 11:32:58 +02:00 (CEST) |

Variant on transcripts
Screenings
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