Variant #0000541682 (NC_000010.10:g.95930939C>T, NM_016341.3:c.1495C>T (PLCE1))
| Chromosome |
10 |
| 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.95930939C>T |
| DNA change (hg38) |
g.94171182C>T |
| Published as |
PLCE1(NM_001165979.1):c.571C>T (p.(Arg191Cys)), PLCE1(NM_016341.3):c.1495C>T (p.R499C), PLCE1(NM_016341.4):c.1495C>T (p.R499C) |
| ISCN |
- |
| DB-ID |
PLCE1_000009 See all 6 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) |
0.00175 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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