Variant #0000305900 (NC_000006.11:g.161137790G>A, NM_000301.3:c.782G>A (PLG))
| Chromosome |
6 |
| 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.161137790G>A |
| DNA change (hg38) |
g.160716758G>A |
| Published as |
PLG(NM_000301.3):c.782G>A (p.R261H), PLG(NM_000301.5):c.782G>A (p.(Arg261His)) |
| ISCN |
- |
| DB-ID |
PLG_000004 See all 2 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland Recognized as participating in HAE-PLG in a Portugese family |
| Reference |
Journal: Dias de Castro 2024 |
| ClinVar ID |
ClinVar-RCV005392468.1 |
| dbSNP ID |
rs4252187 |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
0.0025 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.0025 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-11-05 17:49:45 +01:00 (CET) |

Variant on transcripts
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