List of variants in gene SOS1 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 48

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HGVS	dbSNP	gnomAD frequency
NM_005633.4(SOS1):c.749T>C (p.Val250Ala)	rs139290271	0.00054
NM_005633.4(SOS1):c.698A>G (p.Asn233Ser)	rs144934321	0.00026
NM_005633.4(SOS1):c.3286T>A (p.Ser1096Thr)	rs376722127	0.00017
NM_005633.4(SOS1):c.2966G>A (p.Arg989Lys)	rs202043599	0.00016
NM_005633.4(SOS1):c.3709C>G (p.Pro1237Ala)	rs371408734	0.00016
NM_005633.4(SOS1):c.1668A>C (p.Val556=)	rs376314461	0.00013
NM_005633.4(SOS1):c.3600C>G (p.Asp1200Glu)	rs141594736	0.00013
NM_005633.4(SOS1):c.3946C>G (p.His1316Asp)	rs371024396	0.00013
NM_005633.4(SOS1):c.2165G>A (p.Arg722Lys)	rs142666652	0.00010
NM_005633.4(SOS1):c.1829T>C (p.Ile610Thr)	rs776146535	0.00007
NM_005633.4(SOS1):c.3269C>T (p.Pro1090Leu)	rs730881034	0.00007
NM_005633.4(SOS1):c.1018C>T (p.Pro340Ser)	rs190222208	0.00006
NM_005633.4(SOS1):c.2225T>C (p.Ile742Thr)	rs767494615	0.00006
NM_005633.4(SOS1):c.1490G>A (p.Arg497Gln)	rs371314838	0.00004
NM_005633.4(SOS1):c.162A>G (p.Gln54=)	rs763520126	0.00003
NM_005633.4(SOS1):c.3867G>A (p.Gly1289=)	rs767844484	0.00003
NM_005633.4(SOS1):c.1008A>G (p.Gln336=)	rs1320092319	0.00002
NM_005633.4(SOS1):c.1251A>C (p.Leu417=)	rs144027132	0.00002
NM_005633.4(SOS1):c.396A>T (p.Ala132=)	rs727505385	0.00002
NM_005633.4(SOS1):c.1047C>T (p.His349=)	rs1043516636	0.00001
NM_005633.4(SOS1):c.1278G>A (p.Gln426=)	rs1352756240	0.00001
NM_005633.4(SOS1):c.1719T>C (p.Asp573=)	rs746674452	0.00001
NM_005633.4(SOS1):c.2604T>C (p.Phe868=)	rs756520305	0.00001
NM_005633.4(SOS1):c.2728G>C (p.Asp910His)	rs369277679	0.00001
NM_005633.4(SOS1):c.3060C>T (p.Asn1020=)	rs142431345	0.00001
NM_005633.4(SOS1):c.3093T>C (p.Tyr1031=)	rs766864647	0.00001
NM_005633.4(SOS1):c.3114T>G (p.Pro1038=)	rs777755307	0.00001
NM_005633.4(SOS1):c.3438A>G (p.Glu1146=)	rs1226908698	0.00001
NM_005633.4(SOS1):c.3732T>C (p.His1244=)	rs1391583247	0.00001
NM_005633.4(SOS1):c.3832T>C (p.Leu1278=)	rs750354913	0.00001
NM_005633.4(SOS1):c.429G>A (p.Lys143=)	rs773264070	0.00001
NM_005633.4(SOS1):c.675T>G (p.Val225=)	rs371482290	0.00001
NM_005633.4(SOS1):c.1293T>C (p.Gly431=)
NM_005633.4(SOS1):c.2127T>C (p.Tyr709=)	rs1340535048
NM_005633.4(SOS1):c.214-18A>T
NM_005633.4(SOS1):c.2674-9T>C
NM_005633.4(SOS1):c.2811C>T (p.Ile937=)	rs1668929693
NM_005633.4(SOS1):c.3136A>C (p.Arg1046=)	rs1668859268
NM_005633.4(SOS1):c.3195T>C (p.Tyr1065=)	rs1280224224
NM_005633.4(SOS1):c.3321C>T (p.Ser1107=)
NM_005633.4(SOS1):c.360T>C (p.Tyr120=)
NM_005633.4(SOS1):c.3658G>A (p.Val1220Met)	rs776814547
NM_005633.4(SOS1):c.3709C>A (p.Pro1237Thr)	rs371408734
NM_005633.4(SOS1):c.375G>A (p.Gln125=)	rs1400246247
NM_005633.4(SOS1):c.3876T>C (p.Val1292=)	rs1423591930
NM_005633.4(SOS1):c.396A>G (p.Ala132=)	rs727505385
NM_005633.4(SOS1):c.483T>C (p.Asp161=)	rs1553362598
NM_005633.4(SOS1):c.706T>C (p.Leu236=)	rs1418372765

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