Variant #0000954356 (NC_000005.9:g.176832166G>C, NM_000505.3:c.418C>G (F12))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.176832166G>C
DNA change (hg38) g.177405165G>C
Published as -
ISCN -
DB-ID F12_000020 See all 4 reported entries
Variant remarks Conflicting interpretation of pathogenicity
-1. VUS as introduced by GeneDx, Gaithersburg MA
-2. Likely benign as introduced by CeGaT Center for Human Genetics Tübingen, Germany. Criteria applied: BP4, BS1
-3. Benign as introduced by CeMIA, Larissa Greece
Reference -
ClinVar ID ClinVar-SCV003842612.1
dbSNP ID rs35515200
Origin SUMMARY record
Segregation -
Frequency 0.00247 (gnomAD)
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0022 View details
Owner Christian Drouet
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-12-26 17:49:28 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
F12 NM_000505.3 -?/. 6 c.418C>G r.(?) p.(Leu140Val)


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