ClinVar Miner

List of variants in gene SOS1 reported as uncertain significance for Moyamoya syndrome

Included ClinVar conditions (49):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 129
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HGVS dbSNP
NM_005633.3(SOS1):c.*1094_*1097delTTTG rs886056016
NM_005633.3(SOS1):c.*1224A>G rs886056015
NM_005633.3(SOS1):c.*1303C>A rs115153488
NM_005633.3(SOS1):c.*1309A>G rs145273962
NM_005633.3(SOS1):c.*1385A>G rs868000333
NM_005633.3(SOS1):c.*1589T>G rs886056014
NM_005633.3(SOS1):c.*1678C>A rs886056013
NM_005633.3(SOS1):c.*1684G>C rs886056012
NM_005633.3(SOS1):c.*1694del rs767903412
NM_005633.3(SOS1):c.*2048_*2050dup rs761591990
NM_005633.3(SOS1):c.*2063_*2066dup rs886056011
NM_005633.3(SOS1):c.*2208dup rs886056010
NM_005633.3(SOS1):c.*2218T>A rs886056009
NM_005633.3(SOS1):c.*223C>T rs886056022
NM_005633.3(SOS1):c.*2497G>A rs886056008
NM_005633.3(SOS1):c.*2503_*2506dup rs886056007
NM_005633.3(SOS1):c.*298C>G rs886056021
NM_005633.3(SOS1):c.*3189_*3192del rs572584074
NM_005633.3(SOS1):c.*3416_*3417del rs200892895
NM_005633.3(SOS1):c.*3451A>T rs78411167
NM_005633.3(SOS1):c.*3463A>G rs886056006
NM_005633.3(SOS1):c.*3566_*3568del rs886056005
NM_005633.3(SOS1):c.*3725T>C rs72799430
NM_005633.3(SOS1):c.*3727G>C rs886056004
NM_005633.3(SOS1):c.*4023T>C rs1043800
NM_005633.3(SOS1):c.*4110C>A rs886056003
NM_005633.3(SOS1):c.*4265A>G rs377303107
NM_005633.3(SOS1):c.*4C>T rs188849286
NM_005633.3(SOS1):c.*534C>T rs773935049
NM_005633.3(SOS1):c.*544C>T rs886056020
NM_005633.3(SOS1):c.*642T>C rs886056019
NM_005633.3(SOS1):c.*696G>A rs886056018
NM_005633.3(SOS1):c.*758A>T rs182650589
NM_005633.3(SOS1):c.*766del rs533720751
NM_005633.3(SOS1):c.*855G>A rs886056017
NM_005633.3(SOS1):c.*909G>A rs147219108
NM_005633.3(SOS1):c.1018C>T (p.Pro340Ser) rs190222208
NM_005633.3(SOS1):c.1098T>A (p.Asp366Glu) rs730881040
NM_005633.3(SOS1):c.109A>G (p.Thr37Ala) rs150565592
NM_005633.3(SOS1):c.1385T>A (p.Phe462Tyr) rs730881043
NM_005633.3(SOS1):c.1490G>A (p.Arg497Gln) rs371314838
NM_005633.3(SOS1):c.1564A>C (p.Asn522His) rs761094509
NM_005633.3(SOS1):c.1574T>C (p.Ile525Thr) rs146722878
NM_005633.3(SOS1):c.1659G>A (p.Met553Ile) rs886056025
NM_005633.3(SOS1):c.1720G>A (p.Val574Ile) rs727504641
NM_005633.3(SOS1):c.1727G>T (p.Arg576Ile) rs1553356023
NM_005633.3(SOS1):c.1829T>C (p.Ile610Thr) rs776146535
NM_005633.3(SOS1):c.1989A>C (p.Ile663=) rs587781172
NM_005633.3(SOS1):c.2121T>C (p.Asp707=) rs571408451
NM_005633.3(SOS1):c.225A>G (p.Gln75=) rs560037748
NM_005633.3(SOS1):c.2316G>C (p.Glu772Asp) rs1176763588
NM_005633.3(SOS1):c.233T>G (p.Phe78Cys) rs201352584
NM_005633.3(SOS1):c.2371C>A (p.Leu791Ile) rs142004123
NM_005633.3(SOS1):c.2760G>A (p.Arg920=) rs149092581
NM_005633.3(SOS1):c.2789T>C (p.Phe930Ser) rs886056024
NM_005633.3(SOS1):c.2966G>A (p.Arg989Lys) rs202043599
NM_005633.3(SOS1):c.3032A>G (p.Asn1011Ser) rs8192671
NM_005633.3(SOS1):c.3068C>G (p.Pro1023Arg) rs1572806229
NM_005633.3(SOS1):c.3269C>T (p.Pro1090Leu) rs730881034
NM_005633.3(SOS1):c.3286T>A (p.Ser1096Thr) rs376722127
NM_005633.3(SOS1):c.3290G>C (p.Ser1097Thr) rs727505379
NM_005633.3(SOS1):c.3347-3C>T rs779326746
NM_005633.3(SOS1):c.3392G>A (p.Arg1131Lys) rs768113420
NM_005633.3(SOS1):c.3418T>A (p.Leu1140Ile) rs375550588
NM_005633.3(SOS1):c.3433G>A (p.Asp1145Asn) rs727505383
NM_005633.3(SOS1):c.3585A>G (p.Arg1195=) rs587781173
NM_005633.3(SOS1):c.3624T>C (p.Pro1208=) rs763107563
NM_005633.3(SOS1):c.3658G>A (p.Val1220Met) rs776814547
NM_005633.3(SOS1):c.3709C>G (p.Pro1237Ala) rs371408734
NM_005633.3(SOS1):c.3793T>G (p.Ser1265Ala) rs886056023
NM_005633.3(SOS1):c.487A>G (p.Lys163Glu) rs886042206
NM_005633.3(SOS1):c.553A>G (p.Ile185Val) rs143962515
NM_005633.3(SOS1):c.587C>T (p.Ser196Leu) rs199898869
NM_005633.3(SOS1):c.5A>T (p.Gln2Leu) rs886056026
NM_005633.3(SOS1):c.643T>C (p.Tyr215His) rs730881039
NM_005633.3(SOS1):c.675T>G (p.Val225=) rs371482290
NM_005633.3(SOS1):c.848T>C (p.Phe283Ser) rs1572855029
NM_005633.3(SOS1):c.864+12A>C rs374379005
NM_005633.3(SOS1):c.865-4T>C rs750788947
NM_005633.3(SOS1):c.899G>A (p.Arg300Gln) rs754374236
NM_005633.3(SOS1):c.929G>A (p.Arg310His) rs143481916
NM_005633.3(SOS1):c.979A>G (p.Ile327Val) rs758546951
NM_005633.3(SOS1):c.985G>A (p.Glu329Lys) rs756679265
NM_005633.4(SOS1):c.*1049G>T
NM_005633.4(SOS1):c.*110C>A
NM_005633.4(SOS1):c.*1270T>C
NM_005633.4(SOS1):c.*1391C>T
NM_005633.4(SOS1):c.*1396G>T
NM_005633.4(SOS1):c.*1412A>G
NM_005633.4(SOS1):c.*1477G>A
NM_005633.4(SOS1):c.*1535G>A
NM_005633.4(SOS1):c.*1641A>G
NM_005633.4(SOS1):c.*1762A>C
NM_005633.4(SOS1):c.*185A>G
NM_005633.4(SOS1):c.*1998G>T
NM_005633.4(SOS1):c.*2056A>C
NM_005633.4(SOS1):c.*218T>G
NM_005633.4(SOS1):c.*21A>G
NM_005633.4(SOS1):c.*2246A>T
NM_005633.4(SOS1):c.*2257C>G
NM_005633.4(SOS1):c.*230T>C
NM_005633.4(SOS1):c.*2512C>A
NM_005633.4(SOS1):c.*2662G>A
NM_005633.4(SOS1):c.*2893C>A
NM_005633.4(SOS1):c.*3041A>C
NM_005633.4(SOS1):c.*3149C>T
NM_005633.4(SOS1):c.*3158T>C
NM_005633.4(SOS1):c.*3230T>C
NM_005633.4(SOS1):c.*3252A>C
NM_005633.4(SOS1):c.*3291C>T
NM_005633.4(SOS1):c.*3326T>C
NM_005633.4(SOS1):c.*3750T>C
NM_005633.4(SOS1):c.*3811T>C
NM_005633.4(SOS1):c.*3989G>C
NM_005633.4(SOS1):c.*4014T>C
NM_005633.4(SOS1):c.*4076C>T
NM_005633.4(SOS1):c.*4077G>T
NM_005633.4(SOS1):c.*408C>T
NM_005633.4(SOS1):c.*421A>G
NM_005633.4(SOS1):c.*483A>C
NM_005633.4(SOS1):c.*559C>T
NM_005633.4(SOS1):c.*664C>T
NM_005633.4(SOS1):c.*873C>T
NM_005633.4(SOS1):c.1635G>A (p.Gln545=)
NM_005633.4(SOS1):c.1660C>A (p.Leu554Ile)
NM_005633.4(SOS1):c.2674-7C>T
NM_005633.4(SOS1):c.3592A>G (p.Ile1198Val)
NM_005633.4(SOS1):c.670A>G (p.Lys224Glu)
NM_005633.4(SOS1):c.730A>G (p.Asn244Asp)

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