ClinVar Miner

List of variants in gene SOS1 reported as uncertain significance for Rasopathy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 73
Download table as spreadsheet
HGVS dbSNP
NC_000002.11:g.(?_39278265)_(39347583_?)dup
NC_000002.11:g.(?_39294749)_(39347583_?)dup
NM_005633.3(SOS1):c.1007A>G (p.Gln336Arg) rs765028553
NM_005633.3(SOS1):c.1008A>G (p.Gln336=)
NM_005633.3(SOS1):c.1010A>G (p.Tyr337Cys) rs724160007
NM_005633.3(SOS1):c.1018C>T (p.Pro340Ser) rs190222208
NM_005633.3(SOS1):c.1097A>T (p.Asp366Val)
NM_005633.3(SOS1):c.115G>A (p.Glu39Lys)
NM_005633.3(SOS1):c.1202+5A>G rs1021449471
NM_005633.3(SOS1):c.124G>A (p.Asp42Asn)
NM_005633.3(SOS1):c.1269C>G (p.Asn423Lys) rs138459502
NM_005633.3(SOS1):c.1271A>G (p.Glu424Gly) rs730881042
NM_005633.3(SOS1):c.1276C>A (p.Gln426Lys) rs1558474706
NM_005633.3(SOS1):c.1352C>G (p.Thr451Arg) rs730880218
NM_005633.3(SOS1):c.1370A>G (p.His457Arg) rs1060503524
NM_005633.3(SOS1):c.1490G>A (p.Arg497Gln) rs371314838
NM_005633.3(SOS1):c.1558G>A (p.Asp520Asn)
NM_005633.3(SOS1):c.1646C>A (p.Thr549Lys) rs730881046
NM_005633.3(SOS1):c.1655G>T (p.Arg552Met) rs397517154
NM_005633.3(SOS1):c.1720G>A (p.Val574Ile) rs727504641
NM_005633.3(SOS1):c.1772A>G (p.Asn591Ser) rs757213444
NM_005633.3(SOS1):c.1798A>C (p.Ile600Leu)
NM_005633.3(SOS1):c.1829T>C (p.Ile610Thr) rs776146535
NM_005633.3(SOS1):c.1850T>C (p.Met617Thr) rs775105134
NM_005633.3(SOS1):c.1867T>G (p.Phe623Val) rs727505093
NM_005633.3(SOS1):c.1931T>C (p.Ile644Thr) rs769891933
NM_005633.3(SOS1):c.2010G>C (p.Leu670Phe) rs200712930
NM_005633.3(SOS1):c.2012G>C (p.Ser671Thr) rs1060503525
NM_005633.3(SOS1):c.2089G>T (p.Val697Leu)
NM_005633.3(SOS1):c.2097C>A (p.His699Gln)
NM_005633.3(SOS1):c.2137C>A (p.Arg713=)
NM_005633.3(SOS1):c.2156G>C (p.Gly719Ala) rs200794965
NM_005633.3(SOS1):c.2165G>A (p.Arg722Lys) rs142666652
NM_005633.3(SOS1):c.2167+1G>A rs1558469557
NM_005633.3(SOS1):c.21C>G (p.Pro7=) rs727504845
NM_005633.3(SOS1):c.2312T>C (p.Ile771Thr)
NM_005633.3(SOS1):c.233T>G (p.Phe78Cys) rs201352584
NM_005633.3(SOS1):c.244A>G (p.Ile82Val) rs397517157
NM_005633.3(SOS1):c.2489A>G (p.Asn830Ser) rs397517158
NM_005633.3(SOS1):c.283G>A (p.Glu95Lys) rs1558493384
NM_005633.3(SOS1):c.2944C>A (p.Arg982=) rs1553351455
NM_005633.3(SOS1):c.2966G>A (p.Arg989Lys) rs202043599
NM_005633.3(SOS1):c.3257C>A (p.Pro1086Gln)
NM_005633.3(SOS1):c.3260dup (p.Leu1087fs) rs1558459711
NM_005633.3(SOS1):c.3269C>T (p.Pro1090Leu) rs730881034
NM_005633.3(SOS1):c.3274G>A (p.Ala1092Thr)
NM_005633.3(SOS1):c.3286T>A (p.Ser1096Thr) rs376722127
NM_005633.3(SOS1):c.3322G>A (p.Asp1108Asn) rs199856844
NM_005633.3(SOS1):c.332A>G (p.His111Arg)
NM_005633.3(SOS1):c.3347-1G>A rs141565234
NM_005633.3(SOS1):c.3392G>A (p.Arg1131Lys)
NM_005633.3(SOS1):c.3412A>G (p.Ile1138Val) rs56248239
NM_005633.3(SOS1):c.3418T>A (p.Leu1140Ile) rs375550588
NM_005633.3(SOS1):c.3440T>C (p.Val1147Ala) rs1558455818
NM_005633.3(SOS1):c.350T>G (p.Val117Gly) rs201085754
NM_005633.3(SOS1):c.3598_3599delinsAC (p.Asp1200Thr)
NM_005633.3(SOS1):c.3600C>G (p.Asp1200Glu) rs141594736
NM_005633.3(SOS1):c.3602G>A (p.Arg1201Gln)
NM_005633.3(SOS1):c.3709C>G (p.Pro1237Ala) rs371408734
NM_005633.3(SOS1):c.3721A>G (p.Lys1241Glu) rs367693130
NM_005633.3(SOS1):c.3729C>G (p.Asp1243Glu) rs730881026
NM_005633.3(SOS1):c.3763C>A (p.Pro1255Thr) rs972166211
NM_005633.3(SOS1):c.3778C>G (p.Pro1260Ala) rs779336305
NM_005633.3(SOS1):c.3802G>A (p.Gly1268Ser) rs730881051
NM_005633.3(SOS1):c.3836C>T (p.Thr1279Ile)
NM_005633.3(SOS1):c.3905T>C (p.Ile1302Thr) rs750296853
NM_005633.3(SOS1):c.3946C>G (p.His1316Asp) rs371024396
NM_005633.3(SOS1):c.512T>G (p.Val171Gly) rs397517174
NM_005633.3(SOS1):c.558_562del (p.Leu186fs) rs1553362269
NM_005633.3(SOS1):c.643T>C (p.Tyr215His) rs730881039
NM_005633.3(SOS1):c.746T>C (p.Ile249Thr) rs1324979194
NM_005633.3(SOS1):c.899G>A (p.Arg300Gln) rs754374236
NM_005633.3(SOS1):c.985G>A (p.Glu329Lys) rs756679265

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.