ClinVar Miner

List of variants in gene SOS2 reported as likely benign for not specified

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Total variants: 24
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HGVS dbSNP
NM_006939.4(SOS2):c.1005T>C (p.Tyr335=) rs753698896
NM_006939.4(SOS2):c.1059G>A (p.Glu353=)
NM_006939.4(SOS2):c.1071A>G (p.Gln357=) rs111961549
NM_006939.4(SOS2):c.2007T>C (p.Ser669=) rs577622341
NM_006939.4(SOS2):c.2057+19T>A rs544924513
NM_006939.4(SOS2):c.2190A>G (p.Ser730=)
NM_006939.4(SOS2):c.2317G>C (p.Asp773His) rs114711076
NM_006939.4(SOS2):c.2786-17_2786-16insTC
NM_006939.4(SOS2):c.294A>G (p.Lys98=) rs149713664
NM_006939.4(SOS2):c.3051A>C (p.Arg1017=)
NM_006939.4(SOS2):c.3088A>G (p.Thr1030Ala) rs550680554
NM_006939.4(SOS2):c.3235A>G (p.Thr1079Ala) rs61755576
NM_006939.4(SOS2):c.3250A>G (p.Thr1084Ala) rs150752193
NM_006939.4(SOS2):c.3573T>G (p.Val1191=)
NM_006939.4(SOS2):c.360C>T (p.Tyr120=) rs762044455
NM_006939.4(SOS2):c.3824A>G (p.Tyr1275Cys) rs371619971
NM_006939.4(SOS2):c.3825T>C (p.Tyr1275=)
NM_006939.4(SOS2):c.384A>G (p.Leu128=) rs772264111
NM_006939.4(SOS2):c.3952C>T (p.Pro1318Ser) rs140995728
NM_006939.4(SOS2):c.399A>G (p.Val133=) rs144584870
NM_006939.4(SOS2):c.804T>C (p.Thr268=) rs750437794
NM_006939.4(SOS2):c.813C>T (p.Ser271=)
NM_006939.4(SOS2):c.958C>T (p.Leu320=)
NM_006939.4(SOS2):c.969+20T>G rs559272877

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