Variant #0000859885 (NC_000005.9:g.176831093T>G, NC_000005.9(NM_000505.3):c.1019-2A>C (F12))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.176831093T>G
DNA change (hg38) -
Published as F12(NM_000505.4):c.1019-2A>C
ISCN -
DB-ID F12_000045
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 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2025-10-08 17:11:21 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F12 NM_000505.3 +/. 9i c.1019-2A>C r.spl? p.?
PFN3 NM_001029886.2 +/. _1 c.-3516A>C r.(?) p.(=)


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