List of variants in gene SERPINC1 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000488.4(SERPINC1):c.218C>T (p.Pro73Leu)	rs121909551	0.00092
NM_000488.4(SERPINC1):c.1005G>A (p.Val335=)	rs192187532	0.00031
NM_000488.4(SERPINC1):c.-57G>A	rs372524963	0.00029
NM_000488.4(SERPINC1):c.1265T>C (p.Ile422Thr)	rs772809607	0.00021
NM_000488.4(SERPINC1):c.886G>C (p.Ala296Pro)	rs372820797	0.00005
NM_000488.4(SERPINC1):c.1172G>A (p.Arg391Gln)	rs201541724	0.00004
NM_000488.4(SERPINC1):c.595G>A (p.Gly199Arg)	rs778341415	0.00004
NM_000488.4(SERPINC1):c.100G>A (p.Gly34Arg)	rs773254902	0.00003
NM_000488.4(SERPINC1):c.1256C>T (p.Ala419Val)	rs121909568	0.00001
NM_000488.4(SERPINC1):c.391C>T (p.Leu131Phe)	rs121909567	0.00001
NM_000488.4(SERPINC1):c.408+4C>T	rs201551398	0.00001
NM_000488.4(SERPINC1):c.449A>C (p.Gln150Pro)	rs765445413	0.00001
NM_000488.4(SERPINC1):c.980T>C (p.Val327Ala)	rs773399107	0.00001
NM_000488.4(SERPINC1):c.166C>T (p.Arg56Cys)	rs28929469
NM_000488.4(SERPINC1):c.409-12dup	rs201656611
NM_000488.4(SERPINC1):c.442T>C (p.Ser148Pro)	rs121909569

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.