ClinVar Miner

List of variants in gene SZT2 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001365999.1(SZT2):c.2631C>T (p.Thr877=) rs140831372 0.00717
NM_001365999.1(SZT2):c.4701G>A (p.Leu1567=) rs111932993 0.00598
NM_001365999.1(SZT2):c.4531G>A (p.Val1511Ile) rs76675748 0.00361
NM_001365999.1(SZT2):c.7256G>A (p.Arg2419Gln) rs72637949 0.00103
NM_001365999.1(SZT2):c.4983T>C (p.Asp1661=) rs139810154 0.00098
NM_001365999.1(SZT2):c.4342C>T (p.Arg1448Cys) rs140004653 0.00061
NM_001365999.1(SZT2):c.8944C>T (p.His2982Tyr) rs754779853 0.00045
NM_001365999.1(SZT2):c.6185G>A (p.Arg2062Gln) rs200443293 0.00038
NM_001365999.1(SZT2):c.4963C>T (p.Pro1655Ser) rs144139818 0.00031
NM_001365999.1(SZT2):c.4064A>G (p.His1355Arg) rs149741610 0.00022
NM_001365999.1(SZT2):c.5813T>C (p.Ile1938Thr) rs139028174 0.00017
NM_001365999.1(SZT2):c.653C>T (p.Ser218Leu) rs376862612 0.00013
NM_001365999.1(SZT2):c.4892C>T (p.Thr1631Met) rs201312287 0.00009
NM_001365999.1(SZT2):c.3355C>G (p.Pro1119Ala) rs137956992 0.00004
NM_001365999.1(SZT2):c.5906G>A (p.Arg1969Gln) rs201099906 0.00004
NM_001365999.1(SZT2):c.9880C>T (p.Arg3294Trp) rs199787819 0.00004
NM_001365999.1(SZT2):c.2875C>T (p.Leu959=) rs1570647334 0.00003
NM_001365999.1(SZT2):c.3511G>T (p.Gly1171Trp) rs201767217 0.00003
NM_001365999.1(SZT2):c.2353A>G (p.Ser785Gly) rs754599484 0.00001
NM_001365999.1(SZT2):c.3640C>T (p.Arg1214Ter) rs761810492 0.00001
NM_001365999.1(SZT2):c.5316A>G (p.Glu1772=) rs797046032 0.00001
NM_001365999.1(SZT2):c.9731C>T (p.Pro3244Leu) rs774448705 0.00001
NM_001365999.1(SZT2):c.3019A>T (p.Met1007Leu) rs2153933173
NM_001365999.1(SZT2):c.7874-16C>G rs72883828

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.