ClinVar Miner

List of variants in gene SOS1 reported as benign for not provided

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Gene type:
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Total variants: 21
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HGVS dbSNP
NM_005633.3(SOS1):c.1074+285G>A
NM_005633.3(SOS1):c.1203-307T>C
NM_005633.3(SOS1):c.1770G>A (p.Glu590=) rs553331572
NM_005633.3(SOS1):c.1858+142A>G
NM_005633.3(SOS1):c.1858+302G>C
NM_005633.3(SOS1):c.1941-44C>T
NM_005633.3(SOS1):c.1953A>G (p.Pro651=) rs141507912
NM_005633.3(SOS1):c.1962G>A (p.Glu654=) rs144382701
NM_005633.3(SOS1):c.1964C>T (p.Pro655Leu) rs56219475
NM_005633.3(SOS1):c.2122G>A (p.Ala708Thr) rs140811086
NM_005633.3(SOS1):c.2371C>A (p.Leu791Ile) rs142004123
NM_005633.3(SOS1):c.2511-301_2511-300insCT rs5830552
NM_005633.3(SOS1):c.3081+32A>G rs6723430
NM_005633.3(SOS1):c.3347-243delT rs5830550
NM_005633.3(SOS1):c.3347-318A>G
NM_005633.3(SOS1):c.3357C>T (p.Thr1119=) rs373319212
NM_005633.3(SOS1):c.3391+7A>G rs201982464
NM_005633.3(SOS1):c.345+259_345+262delGTTT rs148203100
NM_005633.3(SOS1):c.553A>G (p.Ile185Val) rs143962515
NM_005633.3(SOS1):c.570C>T (p.Asp190=) rs55980502
NM_005633.3(SOS1):c.864+219G>A

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