ClinVar Miner

List of variants in gene SOS2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_006939.4(SOS2):c.1071A>G (p.Gln357=) rs111961549
NM_006939.4(SOS2):c.1785C>T (p.Gly595=) rs750732217
NM_006939.4(SOS2):c.1934+85_1934+88del rs201762253
NM_006939.4(SOS2):c.2007T>C (p.Ser669=) rs577622341
NM_006939.4(SOS2):c.2057+19T>A rs544924513
NM_006939.4(SOS2):c.2057+19_2057+20del rs111970905
NM_006939.4(SOS2):c.2668-86C>G rs74049160
NM_006939.4(SOS2):c.294A>G (p.Lys98=) rs149713664
NM_006939.4(SOS2):c.2958+197G>T rs145761373
NM_006939.4(SOS2):c.2958+263G>A rs143771743
NM_006939.4(SOS2):c.2958+296G>A rs148973408
NM_006939.4(SOS2):c.3075+131A>G rs58543605
NM_006939.4(SOS2):c.3075+278del rs200433609
NM_006939.4(SOS2):c.3076-25C>T rs74049156
NM_006939.4(SOS2):c.3076-264G>A rs147840816
NM_006939.4(SOS2):c.3235A>G (p.Thr1079Ala) rs61755576
NM_006939.4(SOS2):c.3338-141G>C rs190371489
NM_006939.4(SOS2):c.3338-200T>C rs74744180
NM_006939.4(SOS2):c.346-194G>C rs74542284
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.384A>G (p.Leu128=) rs772264111
NM_006939.4(SOS2):c.399A>G (p.Val133=) rs144584870
NM_006939.4(SOS2):c.511-81G>A rs60775477
NM_006939.4(SOS2):c.714+95G>A rs144846115
NM_006939.4(SOS2):c.804T>C (p.Thr268=) rs750437794
NM_006939.4(SOS2):c.858+40A>G rs148013479
NM_006939.4(SOS2):c.859-66C>G rs7146333
NM_006939.4(SOS2):c.88-142C>A rs148637943
NM_006939.4(SOS2):c.969+181G>T rs55847805
NM_006939.4(SOS2):c.969+20T>G rs559272877

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