List of variants in gene SZT2 reported as uncertain significance for not specified

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001365999.1(SZT2):c.6380A>T (p.Tyr2127Phe)	rs149812437	0.00200
NM_001365999.1(SZT2):c.4727G>A (p.Arg1576His)	rs143935839	0.00119
NM_001365999.1(SZT2):c.8916+8G>A	rs147419780	0.00075
NM_001365999.1(SZT2):c.6343C>G (p.Pro2115Ala)	rs147309177	0.00073
NM_001365999.1(SZT2):c.9887G>T (p.Gly3296Val)	rs368272173	0.00061
NM_001365999.1(SZT2):c.5345C>T (p.Ala1782Val)	rs138028425	0.00034
NM_001365999.1(SZT2):c.2888A>G (p.Lys963Arg)	rs144176855	0.00025
NM_001365999.1(SZT2):c.9172G>A (p.Val3058Met)	rs143959495	0.00024
NM_001365999.1(SZT2):c.4647C>T (p.Gly1549=)	rs149192929	0.00019
NM_001365999.1(SZT2):c.2228A>G (p.His743Arg)	rs545593466	0.00013
NM_001365999.1(SZT2):c.8039G>A (p.Arg2680His)	rs144218947	0.00013
NM_001365999.1(SZT2):c.5772G>T (p.Leu1924=)	rs187188981	0.00011
NM_001365999.1(SZT2):c.9287-8T>C	rs183871754	0.00007
NM_001365999.1(SZT2):c.4503G>A (p.Val1501=)	rs367690658	0.00005
NM_001365999.1(SZT2):c.1272A>G (p.Gln424=)	rs780157180	0.00004
NM_001365999.1(SZT2):c.3466G>A (p.Gly1156Arg)	rs370691670	0.00003
NM_001365999.1(SZT2):c.4113C>G (p.Ser1371Arg)	rs1001442150	0.00003
NM_001365999.1(SZT2):c.4166+4A>G	rs184298720	0.00003
NM_001365999.1(SZT2):c.2477G>A (p.Arg826Gln)	rs752495437	0.00001
NM_001365999.1(SZT2):c.2533C>G (p.Leu845Val)	rs181729793	0.00001
NM_001365999.1(SZT2):c.5316A>G (p.Glu1772=)	rs797046032	0.00001
NM_001365999.1(SZT2):c.7087G>A (p.Gly2363Arg)	rs1557587748
NM_001365999.1(SZT2):c.7512-17dup
NM_001365999.1(SZT2):c.7613G>A (p.Cys2538Tyr)	rs1553153691
NM_001365999.1(SZT2):c.8074A>C (p.Ile2692Leu)
NM_001365999.1(SZT2):c.8182G>C (p.Glu2728Gln)	rs1553154186
NM_001365999.1(SZT2):c.8594C>T (p.Pro2865Leu)	rs374031590
NM_001365999.1(SZT2):c.9636C>G (p.Phe3212Leu)	rs1252399076
NM_001365999.1(SZT2):c.997C>G (p.Pro333Ala)

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