List of variants in gene F9 reported as likely pathogenic by Invitae

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 22

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000133.4(F9):c.1345C>T (p.Arg449Trp)	rs757996262	0.00009
NM_000133.4(F9):c.149G>C (p.Gly50Ala)	rs1229048705	0.00001
NM_000133.4(F9):c.-17A>G	rs1927322926
NM_000133.4(F9):c.1079T>C (p.Phe360Ser)
NM_000133.4(F9):c.1105C>T (p.Leu369Phe)	rs2148367939
NM_000133.4(F9):c.1106T>C (p.Leu369Pro)	rs1603267393
NM_000133.4(F9):c.1174A>G (p.Asn392Asp)	rs1603267412
NM_000133.4(F9):c.1219T>A (p.Cys407Ser)
NM_000133.4(F9):c.1272C>A (p.Phe424Leu)
NM_000133.4(F9):c.1295G>C (p.Gly432Ala)	rs1928130497
NM_000133.4(F9):c.236A>T (p.Glu79Val)
NM_000133.4(F9):c.251C>T (p.Thr84Ile)
NM_000133.4(F9):c.280G>A (p.Gly94Arg)	rs1556437035
NM_000133.4(F9):c.302C>A (p.Pro101Gln)	rs2148357901
NM_000133.4(F9):c.368T>C (p.Phe123Ser)	rs1927592901
NM_000133.4(F9):c.382T>C (p.Cys128Arg)
NM_000133.4(F9):c.482A>G (p.Tyr161Cys)	rs1927768329
NM_000133.4(F9):c.718T>G (p.Trp240Gly)	rs1390220758
NM_000133.4(F9):c.796G>A (p.Ala266Thr)
NM_000133.4(F9):c.835G>C (p.Ala279Pro)	rs137852247
NM_000133.4(F9):c.86C>T (p.Thr29Ile)
NM_000133.4(F9):c.947T>C (p.Ile316Thr)	rs1603267344

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.