Variant #0000244036 (NC_000001.10:g.225136317G>A, NM_000447.2:c.(86G>A) (PSEN2))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.225136317G>A |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PSEN2_000025 |
| Variant remarks |
Observed in one African control individual of the <a href=\""http://www.cephb.fr/en/hgdp/diversity.php/"""" target=blank> Human Genome Diversity Panel</a>. /r/Point mutation in coding region predicting an amino acid substitution"" Variant Error [EREF/EUNCERTAIN]: This genomic variant does not match the reference sequence; the transcript variant also has an error. Please fix this entry and then remove this message. |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Marc Cruts |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2013-05-01 13:44:57 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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