ClinVar Miner

List of variants in gene SOS1 reported as uncertain significance by Integrated Genetics/Laboratory Corporation of America

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_005633.3(SOS1):c.1047C>T (p.His349=) rs1043516636
NM_005633.3(SOS1):c.1278G>A (p.Gln426=) rs1352756240
NM_005633.3(SOS1):c.1352C>G (p.Thr451Arg) rs730880218
NM_005633.3(SOS1):c.1454A>G (p.Asn485Ser) rs140671910
NM_005633.3(SOS1):c.1627T>C (p.Ser543Pro) rs981234810
NM_005633.3(SOS1):c.1646C>A (p.Thr549Lys) rs730881046
NM_005633.3(SOS1):c.1720G>A (p.Val574Ile) rs727504641
NM_005633.3(SOS1):c.1820T>C (p.Ile607Thr) rs758699499
NM_005633.3(SOS1):c.1867T>G (p.Phe623Val) rs727505093
NM_005633.3(SOS1):c.2127T>C (p.Tyr709=) rs1340535048
NM_005633.3(SOS1):c.213+9A>G rs553097014
NM_005633.3(SOS1):c.2188G>T (p.Val730Phe) rs1558469016
NM_005633.3(SOS1):c.2489A>G (p.Asn830Ser) rs397517158
NM_005633.3(SOS1):c.2511-9T>A rs769427441
NM_005633.3(SOS1):c.2606A>G (p.Asn869Ser) rs730881030
NM_005633.3(SOS1):c.2788T>A (p.Phe930Ile) rs1558465734
NM_005633.3(SOS1):c.2791+7_2791+10delATTT rs760707217
NM_005633.3(SOS1):c.2945G>A (p.Arg982Gln) rs1553351453
NM_005633.3(SOS1):c.2999G>A (p.Ser1000Asn) rs891035934
NM_005633.3(SOS1):c.3286T>A (p.Ser1096Thr) rs376722127
NM_005633.3(SOS1):c.3322G>C (p.Asp1108His) rs199856844
NM_005633.3(SOS1):c.3347-1G>A rs141565234
NM_005633.3(SOS1):c.3391+3_3391+6delTAGT rs756201866
NM_005633.3(SOS1):c.3412A>G (p.Ile1138Val) rs56248239
NM_005633.3(SOS1):c.3510+9A>G rs1229357367
NM_005633.3(SOS1):c.3524A>C (p.His1175Pro) rs730881035
NM_005633.3(SOS1):c.3601C>T (p.Arg1201Trp)
NM_005633.3(SOS1):c.3658G>T (p.Val1220Leu) rs776814547
NM_005633.3(SOS1):c.3724A>G (p.Ser1242Gly) rs1293079271
NM_005633.3(SOS1):c.376G>A (p.Val126Ile) rs755770649
NM_005633.3(SOS1):c.3832T>C (p.Leu1278=) rs750354913
NM_005633.3(SOS1):c.3857C>G (p.Ser1286Cys) rs374341202
NM_005633.3(SOS1):c.3857C>T (p.Ser1286Phe) rs374341202
NM_005633.3(SOS1):c.483T>C (p.Asp161=) rs1553362598
NM_005633.3(SOS1):c.510+10T>A rs1553362584
NM_005633.3(SOS1):c.638G>A (p.Arg213Gln) rs374761537
NM_005633.3(SOS1):c.688T>G (p.Phe230Val) rs397517177
NM_005633.3(SOS1):c.706T>C (p.Leu236=) rs1418372765
NM_005633.3(SOS1):c.720T>C (p.Asn240=) rs779699814
NM_005633.3(SOS1):c.755T>C (p.Ile252Thr) rs142094234

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