Variant #0000267943 (NC_000005.9:g.176831826C>G, NM_000505.3:c.619G>C (F12))
| Chromosome |
5 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.176831826C>G |
| DNA change (hg38) |
g.177404825C>G |
| Published as |
F12(NM_000505.4):c.619G>C (p.A207P) |
| ISCN |
- |
| DB-ID |
F12_000005 See all 3 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland. To be noted. Pechnikova 2023 described a 13-year-old girl with symptoms of HAE who is homozygous for the allele encoding FXII-Ala207Pro and speculated that the Pro207 form of FXII may contribute to her symptoms. The patient’s father, who does not exhibit symptoms of HAE, is also homozygous for FXII-Pro207, while her mother is heterozygous for this polymorphism. Shamanaev 2025 shows that there is no obvious difference between FXII-Ala207 and FXII-Pro207 in their capacities to support reciprocal activation and subsquent KKS devlopment. |
| Reference |
Journal: Pechnikova 2023 Journal: Shamanaev 2025 |
| ClinVar ID |
ClinVar-SCV001441476.1 |
| dbSNP ID |
rs17876030 |
| Origin |
CLASSIFICATION record |
| Segregation |
no |
| Frequency |
0.034661 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.94934 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-07-21 12:05:23 +02:00 (CEST) |

Variant on transcripts
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