ClinVar Miner

List of variants in gene SEMA4F reported as uncertain significance by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_004263.5(SEMA4F):c.2204G>A (p.Ser735Asn) rs113159774 0.00086
NM_004263.5(SEMA4F):c.971C>T (p.Pro324Leu) rs192986592 0.00050
NM_004263.5(SEMA4F):c.1828C>T (p.Arg610Trp) rs367999393 0.00022
NM_004263.5(SEMA4F):c.1312G>A (p.Val438Met) rs373374527 0.00012
NM_004263.5(SEMA4F):c.2180C>T (p.Pro727Leu) rs149150975 0.00011
NM_004263.5(SEMA4F):c.1859C>T (p.Pro620Leu) rs145357480 0.00008
NM_004263.5(SEMA4F):c.1963C>T (p.Arg655Trp) rs149518003 0.00007
NM_004263.5(SEMA4F):c.1106T>C (p.Leu369Pro) rs776442238 0.00005
NM_004263.5(SEMA4F):c.599C>G (p.Pro200Arg) rs1287924286 0.00005
NM_004263.5(SEMA4F):c.1366G>A (p.Gly456Arg) rs780796123 0.00004
NM_004263.5(SEMA4F):c.772T>C (p.Phe258Leu) rs181221221 0.00004
NM_004263.5(SEMA4F):c.1040C>T (p.Pro347Leu) rs746103016 0.00003
NM_004263.5(SEMA4F):c.2146C>T (p.Pro716Ser) rs765852749 0.00003
NM_004263.5(SEMA4F):c.947G>A (p.Arg316Gln) rs776046741 0.00003
NM_004263.5(SEMA4F):c.1544G>A (p.Arg515His) rs778118707 0.00002
NM_004263.5(SEMA4F):c.2227C>G (p.Pro743Ala) rs374314667 0.00002
NM_004263.5(SEMA4F):c.835G>A (p.Gly279Ser) rs771416005 0.00002
NM_004263.5(SEMA4F):c.1174C>T (p.Arg392Trp) rs1363385772 0.00001
NM_004263.5(SEMA4F):c.1208G>A (p.Arg403His) rs139378944 0.00001
NM_004263.5(SEMA4F):c.1742C>T (p.Ala581Val) rs746601691 0.00001
NM_004263.5(SEMA4F):c.2047C>T (p.Arg683Cys) rs775752097 0.00001
NM_004263.5(SEMA4F):c.2293T>C (p.Cys765Arg) rs954381707 0.00001
NM_004263.5(SEMA4F):c.241G>A (p.Ala81Thr) rs371410540 0.00001
NM_004263.5(SEMA4F):c.371A>G (p.Asn124Ser) rs763504920 0.00001
NM_004263.5(SEMA4F):c.500G>A (p.Arg167Gln) rs778626481 0.00001
NM_004263.5(SEMA4F):c.516T>A (p.Phe172Leu) rs781411561 0.00001
NM_004263.5(SEMA4F):c.528G>T (p.Gln176His) rs780356014 0.00001
NM_004263.5(SEMA4F):c.616G>A (p.Val206Met) rs766475722 0.00001
NM_004263.5(SEMA4F):c.718G>A (p.Asp240Asn) rs1434858663 0.00001
NM_004263.5(SEMA4F):c.1065T>A (p.Asn355Lys)
NM_004263.5(SEMA4F):c.1226G>A (p.Arg409Gln)
NM_004263.5(SEMA4F):c.1258C>T (p.Pro420Ser)
NM_004263.5(SEMA4F):c.1400G>A (p.Arg467Gln)
NM_004263.5(SEMA4F):c.1420G>A (p.Val474Ile)
NM_004263.5(SEMA4F):c.1444C>T (p.Pro482Ser)
NM_004263.5(SEMA4F):c.1478A>G (p.Tyr493Cys)
NM_004263.5(SEMA4F):c.1520A>G (p.Gln507Arg)
NM_004263.5(SEMA4F):c.1598G>A (p.Ser533Asn)
NM_004263.5(SEMA4F):c.1604G>A (p.Arg535Gln)
NM_004263.5(SEMA4F):c.1640G>A (p.Arg547Gln)
NM_004263.5(SEMA4F):c.167G>T (p.Arg56Leu)
NM_004263.5(SEMA4F):c.1705C>T (p.Arg569Cys)
NM_004263.5(SEMA4F):c.173C>G (p.Ala58Gly) rs775052431
NM_004263.5(SEMA4F):c.1825C>A (p.Pro609Thr) rs2530980779
NM_004263.5(SEMA4F):c.182A>G (p.His61Arg) rs1190946045
NM_004263.5(SEMA4F):c.1852G>T (p.Val618Leu) rs1400811555
NM_004263.5(SEMA4F):c.1909C>T (p.His637Tyr) rs753109312
NM_004263.5(SEMA4F):c.1949G>A (p.Arg650Gln) rs138175347
NM_004263.5(SEMA4F):c.1991C>T (p.Ala664Val)
NM_004263.5(SEMA4F):c.2003T>C (p.Leu668Ser)
NM_004263.5(SEMA4F):c.2057G>A (p.Arg686Gln) rs774869919
NM_004263.5(SEMA4F):c.2074C>T (p.Leu692Phe)
NM_004263.5(SEMA4F):c.2156C>A (p.Pro719His) rs572401608
NM_004263.5(SEMA4F):c.2169T>G (p.Asp723Glu)
NM_004263.5(SEMA4F):c.2248C>G (p.Pro750Ala) rs1685533545
NM_004263.5(SEMA4F):c.2249C>T (p.Pro750Leu)
NM_004263.5(SEMA4F):c.224A>G (p.His75Arg) rs1257734830
NM_004263.5(SEMA4F):c.2266C>T (p.Arg756Trp)
NM_004263.5(SEMA4F):c.2281C>T (p.Pro761Ser) rs1685537302
NM_004263.5(SEMA4F):c.229C>G (p.Leu77Val)
NM_004263.5(SEMA4F):c.259G>A (p.Ala87Thr)
NM_004263.5(SEMA4F):c.293G>A (p.Arg98His)
NM_004263.5(SEMA4F):c.332A>G (p.Asn111Ser) rs1325027056
NM_004263.5(SEMA4F):c.474G>C (p.Gln158His)
NM_004263.5(SEMA4F):c.503G>A (p.Gly168Glu) rs369113935
NM_004263.5(SEMA4F):c.556G>T (p.Val186Phe) rs772525461
NM_004263.5(SEMA4F):c.593C>T (p.Thr198Met)
NM_004263.5(SEMA4F):c.598C>T (p.Pro200Ser)
NM_004263.5(SEMA4F):c.628G>A (p.Glu210Lys)
NM_004263.5(SEMA4F):c.664C>A (p.Leu222Met)
NM_004263.5(SEMA4F):c.800C>T (p.Pro267Leu) rs1328050720
NM_004263.5(SEMA4F):c.811C>T (p.Arg271Cys)
NM_004263.5(SEMA4F):c.839G>A (p.Arg280Gln)
NM_004263.5(SEMA4F):c.866C>T (p.Thr289Met)
NM_004263.5(SEMA4F):c.995C>G (p.Ser332Cys) rs546288150

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