Variant #0000293895 (NC_000008.10:g.145024578G>A, NC_000008.10(NM_000445.3):c.194-11718C>T (PLEC))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.145024578G>A |
| DNA change (hg38) |
g.143950410G>A |
| Published as |
PLEC(NM_201380.2):c.297C>T (p.(Arg99=)), PLEC(NM_201380.4):c.297C>T (p.R99=) |
| ISCN |
- |
| DB-ID |
PLEC_000226 See all 3 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) |
0.00768 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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