List of variants in gene SOS2 studied for Noonan syndrome

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 92

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HGVS	dbSNP
NM_006939.4(SOS2):c.1071A>G (p.Gln357=)	rs111961549
NM_006939.4(SOS2):c.1126A>T (p.Thr376Ser)
NM_006939.4(SOS2):c.1127C>G (p.Thr376Ser)	rs869320687
NM_006939.4(SOS2):c.1146A>G (p.Gln382=)	rs1178247373
NM_006939.4(SOS2):c.1176T>C (p.Tyr392=)	rs1555370242
NM_006939.4(SOS2):c.1198G>A (p.Asp400Asn)	rs200368064
NM_006939.4(SOS2):c.1344G>A (p.Leu448=)	rs35530861
NM_006939.4(SOS2):c.1429C>T (p.Arg477Trp)	rs1555370121
NM_006939.4(SOS2):c.1448G>A (p.Ser483Asn)	rs17122201
NM_006939.4(SOS2):c.147A>G (p.Glu49=)	rs1030329651
NM_006939.4(SOS2):c.1521G>T (p.Glu507Asp)	rs141604342
NM_006939.4(SOS2):c.1861T>G (p.Phe621Val)	rs1555370029
NM_006939.4(SOS2):c.1868G>A (p.Arg623His)	rs138459515
NM_006939.4(SOS2):c.2014C>A (p.Leu672Ile)	rs34139502
NM_006939.4(SOS2):c.2120A>G (p.Glu707Gly)	rs369462490
NM_006939.4(SOS2):c.2128G>C (p.Glu710Gln)	rs768829374
NM_006939.4(SOS2):c.2154T>C (p.Ser718=)	rs568511771
NM_006939.4(SOS2):c.2161+10A>G	rs201629454
NM_006939.4(SOS2):c.2162-10C>T	rs375702667
NM_006939.4(SOS2):c.2162-4C>A	rs57179949
NM_006939.4(SOS2):c.2168C>T (p.Ala723Val)	rs1566827698
NM_006939.4(SOS2):c.2217G>A (p.Lys739=)	rs186110427
NM_006939.4(SOS2):c.2221G>A (p.Ala741Thr)
NM_006939.4(SOS2):c.2246A>G (p.Asn749Ser)	rs761689009
NM_006939.4(SOS2):c.2261G>A (p.Ser754Asn)
NM_006939.4(SOS2):c.2268T>G (p.Pro756=)	rs1555369534
NM_006939.4(SOS2):c.2304G>T (p.Gln768His)
NM_006939.4(SOS2):c.2317G>C (p.Asp773His)	rs114711076
NM_006939.4(SOS2):c.2366T>C (p.Leu789Ser)
NM_006939.4(SOS2):c.2384+5A>G	rs376903120
NM_006939.4(SOS2):c.2396C>T (p.Pro799Leu)
NM_006939.4(SOS2):c.2443A>G (p.Asn815Asp)	rs886041958
NM_006939.4(SOS2):c.2520A>G (p.Ala840=)	rs775682587
NM_006939.4(SOS2):c.257C>T (p.Ala86Val)
NM_006939.4(SOS2):c.2600A>G (p.Asn867Ser)	rs561495878
NM_006939.4(SOS2):c.2602G>A (p.Gly868Ser)	rs751419448
NM_006939.4(SOS2):c.2604C>T (p.Gly868=)	rs765945171
NM_006939.4(SOS2):c.2605G>A (p.Val869Ile)
NM_006939.4(SOS2):c.2606T>C (p.Val869Ala)
NM_006939.4(SOS2):c.2625A>T (p.Ala875=)	rs761442415
NM_006939.4(SOS2):c.2640A>G (p.Ser880=)	rs146730136
NM_006939.4(SOS2):c.2758A>G (p.Ile920Val)
NM_006939.4(SOS2):c.2854G>A (p.Asp952Asn)	rs200387871
NM_006939.4(SOS2):c.290G>A (p.Arg97Gln)
NM_006939.4(SOS2):c.2957G>A (p.Arg986Lys)	rs772746106
NM_006939.4(SOS2):c.2969A>G (p.Glu990Gly)
NM_006939.4(SOS2):c.2983A>G (p.Met995Val)
NM_006939.4(SOS2):c.3066A>G (p.Pro1022=)	rs201696354
NM_006939.4(SOS2):c.3075+7C>T	rs144391749
NM_006939.4(SOS2):c.3088A>G (p.Thr1030Ala)	rs550680554
NM_006939.4(SOS2):c.3235A>G (p.Thr1079Ala)	rs61755576
NM_006939.4(SOS2):c.3250A>G (p.Thr1084Ala)	rs150752193
NM_006939.4(SOS2):c.3266C>A (p.Pro1089Gln)
NM_006939.4(SOS2):c.3275C>T (p.Pro1092Leu)
NM_006939.4(SOS2):c.3338-4A>G	rs777684425
NM_006939.4(SOS2):c.3383C>G (p.Ser1128Cys)	rs1566815476
NM_006939.4(SOS2):c.3403A>G (p.Ser1135Gly)
NM_006939.4(SOS2):c.3490-13_3490-12dup	rs10658395
NM_006939.4(SOS2):c.3503C>A (p.Ser1168Tyr)	rs143166880
NM_006939.4(SOS2):c.3530C>T (p.Pro1177Leu)	rs1566814839
NM_006939.4(SOS2):c.3540_3542TCC[4] (p.Pro1183dup)	rs765097073
NM_006939.4(SOS2):c.3560C>T (p.Pro1187Leu)
NM_006939.4(SOS2):c.3584C>T (p.Ala1195Val)	rs753151750
NM_006939.4(SOS2):c.3744G>T (p.Trp1248Cys)	rs138133010
NM_006939.4(SOS2):c.3755_3757del (p.Ile1252del)	rs775506222
NM_006939.4(SOS2):c.3761C>G (p.Thr1254Arg)	rs772587016
NM_006939.4(SOS2):c.3769A>G (p.Asn1257Asp)	rs150393358
NM_006939.4(SOS2):c.3781A>C (p.Thr1261Pro)	rs1555367637
NM_006939.4(SOS2):c.3830T>C (p.Leu1277Pro)	rs146802994
NM_006939.4(SOS2):c.3952C>T (p.Pro1318Ser)	rs140995728
NM_006939.4(SOS2):c.432G>A (p.Leu144=)
NM_006939.4(SOS2):c.496A>G (p.Met166Val)	rs1555322175
NM_006939.4(SOS2):c.533A>C (p.Gln178Pro)	rs1273376869
NM_006939.4(SOS2):c.549G>C (p.Leu183Phe)	rs137961578
NM_006939.4(SOS2):c.572C>G (p.Pro191Arg)	rs72681869
NM_006939.4(SOS2):c.591A>G (p.Leu197=)	rs113460230
NM_006939.4(SOS2):c.600T>C (p.Tyr200=)	rs766470992
NM_006939.4(SOS2):c.621C>T (p.Ile207=)	rs147109760
NM_006939.4(SOS2):c.622G>A (p.Ala208Thr)	rs61755579
NM_006939.4(SOS2):c.622G>T (p.Ala208Ser)	rs61755579
NM_006939.4(SOS2):c.674G>A (p.Arg225Gln)	rs780580623
NM_006939.4(SOS2):c.714T>G (p.Ser238=)
NM_006939.4(SOS2):c.721G>A (p.Glu241Lys)
NM_006939.4(SOS2):c.780G>T (p.Leu260Phe)	rs1348457314
NM_006939.4(SOS2):c.791C>A (p.Thr264Lys)
NM_006939.4(SOS2):c.800T>A (p.Met267Lys)	rs797045167
NM_006939.4(SOS2):c.800T>G (p.Met267Arg)
NM_006939.4(SOS2):c.816T>C (p.Ser272=)	rs35396088
NM_006939.4(SOS2):c.837C>T (p.Ser279=)	rs542617984
NM_006939.4(SOS2):c.839G>C (p.Cys280Ser)
NM_006939.4(SOS2):c.858+9A>G	rs201701595
NM_006939.4(SOS2):c.859-10A>T	rs761341096

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