Variant #0001014421 (NC_000008.10:g.144997503G>A, NM_000445.3:c.6675C>T (PLEC))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.144997503G>A |
| DNA change (hg38) |
- |
| Published as |
PLEC(NM_000445.3):c.6675C>T (p.(Thr2225=)), PLEC(NM_201380.3):c.7005C>T (p.T2335=), PLEC(NM_201380.4):c.7005C>T (p.T2335=) |
| ISCN |
- |
| DB-ID |
PLEC_000108 See all 5 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00131 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2024-10-29 21:08:56 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|