ClinVar Miner

List of variants in gene SOS1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_005633.4(SOS1):c.*3451A>T rs78411167 0.00429
NM_005633.4(SOS1):c.*758A>T rs182650589 0.00372
NM_005633.4(SOS1):c.*2517C>T rs150628082 0.00321
NM_005633.4(SOS1):c.*1309A>G rs145273962 0.00319
NM_005633.4(SOS1):c.*4023T>C rs1043800 0.00233
NM_005633.4(SOS1):c.570C>T (p.Asp190=) rs55980502 0.00233
NM_005633.4(SOS1):c.3032A>G (p.Asn1011Ser) rs8192671 0.00164
NM_005633.4(SOS1):c.2988G>A (p.Pro996=) rs35462677 0.00156
NM_005633.4(SOS1):c.*534C>T rs773935049 0.00089
NM_005633.4(SOS1):c.3391+7A>G rs201982464 0.00066
NM_005633.4(SOS1):c.2371C>A (p.Leu791Ile) rs142004123 0.00053
NM_005633.4(SOS1):c.*4C>T rs188849286 0.00018
NM_005633.4(SOS1):c.109A>G (p.Thr37Ala) rs150565592 0.00016
NM_005633.4(SOS1):c.1953A>G (p.Pro651=) rs141507912 0.00013
NM_005633.4(SOS1):c.3600C>G (p.Asp1200Glu) rs141594736 0.00013
NM_005633.4(SOS1):c.2165G>A (p.Arg722Lys) rs142666652 0.00010
NM_005633.4(SOS1):c.3269C>T (p.Pro1090Leu) rs730881034 0.00007
NM_005633.4(SOS1):c.1859-3T>C rs199727062 0.00004
NM_005633.4(SOS1):c.3857C>T (p.Ser1286Phe) rs374341202 0.00004
NM_005633.4(SOS1):c.1191A>G (p.Lys397=) rs770175415 0.00001
NM_005633.4(SOS1):c.3105A>C (p.Leu1035=) rs749104275 0.00001
NM_005633.4(SOS1):c.3303T>C (p.Val1101=) rs397517165 0.00001
NM_005633.4(SOS1):c.552T>C (p.Asn184=) rs727503438 0.00001
NM_005633.4(SOS1):c.798A>C (p.Thr266=) rs756044708 0.00001
NM_005633.4(SOS1):c.*1694del rs767903412
NM_005633.4(SOS1):c.*3149C>T rs541644361
NM_005633.4(SOS1):c.*3189_*3192del rs572584074
NM_005633.4(SOS1):c.*400_*401insCAA
NM_005633.4(SOS1):c.1347T>C (p.Thr449=)
NM_005633.4(SOS1):c.2499G>A (p.Leu833=)
NM_005633.4(SOS1):c.2499G>T (p.Leu833=)
NM_005633.4(SOS1):c.2791+4A>G
NM_005633.4(SOS1):c.3258G>A (p.Pro1086=) rs770550039
NM_005633.4(SOS1):c.3597A>C (p.Ser1199=)

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