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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F12 NM_000505.3 -?/-? 7 c.619G>C r.(?) p.(Ala207Pro)
PFN3 NM_001029886.2 -/. - c.-4249G>C r.(?) p.(=)


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