List of variants in gene SEMA3E reported as uncertain significance 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 35

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HGVS	dbSNP	gnomAD frequency
NM_012431.3(SEMA3E):c.155C>G (p.Pro52Arg)	rs370543242	0.00013
NM_012431.3(SEMA3E):c.1290A>T (p.Lys430Asn)	rs61729605	0.00008
NM_012431.3(SEMA3E):c.2133G>T (p.Lys711Asn)	rs768818178	0.00008
NM_012431.3(SEMA3E):c.1076A>G (p.His359Arg)	rs373965521	0.00006
NM_012431.3(SEMA3E):c.1856G>A (p.Arg619His)	rs140160399	0.00006
NM_012431.3(SEMA3E):c.196T>C (p.Tyr66His)	rs558904762	0.00005
NM_012431.3(SEMA3E):c.949A>T (p.Thr317Ser)	rs752718717	0.00005
NM_012431.3(SEMA3E):c.1043G>A (p.Ser348Asn)	rs1293541067	0.00004
NM_012431.3(SEMA3E):c.1048C>T (p.Arg350Trp)	rs546414937	0.00004
NM_012431.3(SEMA3E):c.1147G>T (p.Ala383Ser)	rs373711827	0.00004
NM_012431.3(SEMA3E):c.1909C>G (p.Leu637Val)	rs771976054	0.00004
NM_012431.3(SEMA3E):c.2279G>A (p.Arg760His)	rs143423970	0.00004
NM_012431.3(SEMA3E):c.355G>C (p.Val119Leu)	rs145267516	0.00004
NM_012431.3(SEMA3E):c.2054A>G (p.Asp685Gly)	rs747326285	0.00003
NM_012431.3(SEMA3E):c.1172A>T (p.Tyr391Phe)	rs753965043	0.00002
NM_012431.3(SEMA3E):c.1500+5G>A	rs201772961	0.00002
NM_012431.3(SEMA3E):c.266G>A (p.Gly89Asp)	rs773688938	0.00002
NM_012431.3(SEMA3E):c.335C>T (p.Ala112Val)	rs780025635	0.00002
NM_012431.3(SEMA3E):c.659G>A (p.Arg220His)	rs150833995	0.00002
NM_012431.3(SEMA3E):c.1049G>A (p.Arg350Gln)	rs748722795	0.00001
NM_012431.3(SEMA3E):c.1075C>G (p.His359Asp)	rs1378507372	0.00001
NM_012431.3(SEMA3E):c.1918C>T (p.Leu640Phe)	rs1246755098	0.00001
NM_012431.3(SEMA3E):c.1991C>T (p.Thr664Met)	rs375536813	0.00001
NM_012431.3(SEMA3E):c.2053G>A (p.Asp685Asn)	rs768606535	0.00001
NM_012431.3(SEMA3E):c.233T>C (p.Val78Ala)	rs765517064	0.00001
NM_012431.3(SEMA3E):c.999-10T>C	rs371994521	0.00001
NM_012431.3(SEMA3E):c.1009C>T (p.Arg337Ter)	rs965528935
NM_012431.3(SEMA3E):c.1177A>T (p.Thr393Ser)	rs1027331615
NM_012431.3(SEMA3E):c.1296C>A (p.Asn432Lys)	rs769637710
NM_012431.3(SEMA3E):c.1498C>T (p.Arg500Trp)	rs111300014
NM_012431.3(SEMA3E):c.1630T>C (p.Cys544Arg)	rs2115581814
NM_012431.3(SEMA3E):c.2159G>C (p.Ser720Thr)	rs372156795
NM_012431.3(SEMA3E):c.320T>A (p.Met107Lys)	rs1429296509
NM_012431.3(SEMA3E):c.781G>A (p.Ala261Thr)	rs773917768
NM_012431.3(SEMA3E):c.957T>G (p.Asp319Glu)	rs763045418

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