ClinVar Miner

List of variants in gene SEMA3A reported as uncertain significance for not provided

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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_006080.3(SEMA3A):c.458A>G (p.Asn153Ser) rs139295139 0.00254
NM_006080.3(SEMA3A):c.1198A>G (p.Ile400Val) rs36026860 0.00100
NM_006080.3(SEMA3A):c.196C>T (p.Arg66Trp) rs199979628 0.00043
NM_006080.3(SEMA3A):c.1382T>C (p.Val461Ala) rs144690677 0.00014
NM_006080.3(SEMA3A):c.2062A>G (p.Thr688Ala) rs318240751 0.00013
NM_006080.3(SEMA3A):c.1910G>A (p.Arg637His) rs766918295 0.00011
NM_006080.3(SEMA3A):c.1654C>T (p.Arg552Cys) rs557001005 0.00008
NM_006080.3(SEMA3A):c.1372G>A (p.Val458Ile) rs553661856 0.00004
NM_006080.3(SEMA3A):c.2198G>A (p.Arg733His) rs318240753 0.00004
NM_006080.3(SEMA3A):c.1256G>A (p.Arg419His) rs140701193 0.00002
NM_006080.3(SEMA3A):c.1141-10_1141-8dup rs757969344 0.00001
GRCh37/hg19 7q21.11(chr7:83506642-83638818)x1
GRCh37/hg19 7q21.11(chr7:83593776-83646626)x3
GRCh37/hg19 7q21.11(chr7:83635356-84075096)x1
GRCh37/hg19 7q21.11(chr7:83652875-84395557)x1
GRCh37/hg19 7q21.11(chr7:83678951-83760987)x1
GRCh37/hg19 7q21.11(chr7:83744959-84240868)x3
GRCh37/hg19 7q21.11(chr7:83821768-83892545)x1
NC_000007.14:g.84195026GA[12] rs60880561
NC_000007.14:g.84195026GA[13] rs60880561
NM_006080.3(SEMA3A):c.1102C>T (p.Pro368Ser)
NM_006080.3(SEMA3A):c.1121C>A (p.Pro374His)
NM_006080.3(SEMA3A):c.1141-5_1141-2dup
NM_006080.3(SEMA3A):c.1219C>T (p.Pro407Ser)
NM_006080.3(SEMA3A):c.1393C>T (p.Pro465Ser)
NM_006080.3(SEMA3A):c.1450C>T (p.Arg484Trp)
NM_006080.3(SEMA3A):c.1457C>T (p.Pro486Leu) rs746014457
NM_006080.3(SEMA3A):c.1471G>A (p.Ala491Thr)
NM_006080.3(SEMA3A):c.1495-13A>T
NM_006080.3(SEMA3A):c.1543C>T (p.His515Tyr)
NM_006080.3(SEMA3A):c.1546C>T (p.Arg516Trp)
NM_006080.3(SEMA3A):c.1623A>G (p.Ala541=)
NM_006080.3(SEMA3A):c.1849C>T (p.Arg617Ter)
NM_006080.3(SEMA3A):c.1870G>A (p.Asp624Asn)
NM_006080.3(SEMA3A):c.1926G>T (p.Lys642Asn) rs1229736172
NM_006080.3(SEMA3A):c.1950T>G (p.His650Gln)
NM_006080.3(SEMA3A):c.1952C>A (p.Ala651Glu)
NM_006080.3(SEMA3A):c.1960C>T (p.His654Tyr) rs1404238314
NM_006080.3(SEMA3A):c.2020G>A (p.Glu674Lys)
NM_006080.3(SEMA3A):c.2030T>A (p.Leu677His)
NM_006080.3(SEMA3A):c.2150_2151inv (p.Thr717Met)
NM_006080.3(SEMA3A):c.2200C>T (p.Arg734Trp)
NM_006080.3(SEMA3A):c.2257A>C (p.Asn753His)
NM_006080.3(SEMA3A):c.229A>G (p.Ile77Val)
NM_006080.3(SEMA3A):c.366_367delinsTA (p.Lys122_Ala123delinsAsnThr) rs2115940734
NM_006080.3(SEMA3A):c.453+5C>T
NM_006080.3(SEMA3A):c.456C>G (p.Asp152Glu)
NM_006080.3(SEMA3A):c.506G>A (p.Ser169Asn)
NM_006080.3(SEMA3A):c.514G>A (p.Asp172Asn)
NM_006080.3(SEMA3A):c.58G>A (p.Ala20Thr)
NM_006080.3(SEMA3A):c.625C>G (p.His209Asp)
NM_006080.3(SEMA3A):c.629C>G (p.Pro210Arg) rs1554399881
NM_006080.3(SEMA3A):c.669T>A (p.Asp223Glu)
NM_006080.3(SEMA3A):c.73G>A (p.Gly25Arg)
NM_006080.3(SEMA3A):c.922C>A (p.Leu308Met)

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