"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "SOS2"[g - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 859843	NM_006939.4(SOS2):c.3997T>C (p.Ter1333Arg)	SOS2	Single nucleotide variant (stop lost)	Noonan syndrome 9 +1 more	GUncertain significance
Select item 2057717	NM_006939.4(SOS2):c.3996A>G (p.Gln1332=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 1472803	NM_006939.4(SOS2):c.3987A>C (p.Glu1329Asp)	SOS2 (E1329D)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GConflicting classifications of pathogenicity
Select item 1605815	NM_006939.4(SOS2):c.3984A>G (p.Ala1328=)	SOS2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 766308	NM_006939.4(SOS2):c.3981T>C (p.Asn1327=)	SOS2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 2834961	NM_006939.4(SOS2):c.3980del (p.Asn1327fs)	SOS2 (N1294fs +1 more)	Deletion (frameshift variant)	Noonan syndrome 9	GUncertain significance
Select item 1736640	NM_006939.4(SOS2):c.3975A>G (p.Leu1325=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9 +1 more	GLikely benign
Select item 280784	NM_006939.4(SOS2):c.3968C>T (p.Pro1323Leu)	SOS2 (P1323L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 1383405	NM_006939.4(SOS2):c.3960C>T (p.Tyr1320=)	SOS2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1383572	NM_006939.4(SOS2):c.3958T>C (p.Tyr1320His)	SOS2 (Y1320H)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GUncertain significance
Select item 1063333	NM_006939.4(SOS2):c.3957G>T (p.Leu1319Phe)	SOS2 (L1319F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1107037	NM_006939.4(SOS2):c.3954A>G (p.Pro1318=)	SOS2	Single nucleotide variant (synonymous variant)	not specified +2 more	GLikely benign
Select item 2758991	NM_006939.4(SOS2):c.3953C>A (p.Pro1318Gln)	SOS2 (P1318Q +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 3021082	NM_006939.4(SOS2):c.3952C>G (p.Pro1318Ala)	SOS2 (P1285A +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GBenign
Select item 2797011	NM_006939.4(SOS2):c.3952C>A (p.Pro1318Thr)	SOS2 (P1285T +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 475758	NM_006939.4(SOS2):c.3952C>T (p.Pro1318Ser)	SOS2 (P1318S)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +3 more	GBenign/Likely benign
Select item 2200414	NM_006939.4(SOS2):c.3951C>G (p.Pro1317=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 2059055	NM_006939.4(SOS2):c.3951C>T (p.Pro1317=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9 +1 more	GLikely benign
Select item 721084	NM_006939.4(SOS2):c.3945G>A (p.Ser1315=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9 +1 more	GLikely benign
Select item 1022197	NM_006939.4(SOS2):c.3944C>T (p.Ser1315Leu)	SOS2 (S1315L)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 2060710	NM_006939.4(SOS2):c.3935G>A (p.Arg1312Gln)	SOS2 (R1279Q +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GConflicting classifications of pathogenicity
Select item 2868272	NM_006939.4(SOS2):c.3934C>T (p.Arg1312Trp)	SOS2 (R1312W +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1671341	NM_006939.4(SOS2):c.3934C>A (p.Arg1312=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9 +1 more	GBenign/Likely benign
Select item 1388134	NM_006939.4(SOS2):c.3930C>G (p.Tyr1310Ter)	SOS2 (Y1310*)	Single nucleotide variant (nonsense)	Noonan syndrome 9	GUncertain significance
Select item 2030506	NM_006939.4(SOS2):c.3920del (p.Pro1307fs)	SOS2 (P1307fs +1 more)	Deletion (frameshift variant)	Noonan syndrome 9	GUncertain significance
Select item 1022639	NM_006939.4(SOS2):c.3902A>G (p.His1301Arg)	SOS2 (H1301R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 2727863	NM_006939.4(SOS2):c.3901C>T (p.His1301Tyr)	SOS2 (H1268Y +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GLikely benign
Select item 2563216	NM_006939.4(SOS2):c.3898C>T (p.Pro1300Ser)	SOS2 (P1267S +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GUncertain significance
Select item 2033839	NM_006939.4(SOS2):c.3872_3873del (p.Pro1291fs)	SOS2 (P1291fs +1 more)	Deletion (frameshift variant)	Noonan syndrome 9	GUncertain significance
Select item 1516805	NM_006939.4(SOS2):c.3869C>A (p.Pro1290His)	SOS2 (P1290H)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1009041	NM_006939.4(SOS2):c.3868C>G (p.Pro1290Ala)	SOS2 (P1290A)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GUncertain significance
Select item 2683251	NM_006939.4(SOS2):c.3862C>T (p.Pro1288Ser)	SOS2 (P1255S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2107374	NM_006939.4(SOS2):c.3850C>G (p.Leu1284Val)	SOS2 (L1251V +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2082984	NM_006939.4(SOS2):c.3849T>C (p.Asn1283=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 948367	NM_006939.4(SOS2):c.3845A>G (p.Asn1282Ser)	SOS2 (N1282S)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1932100	NM_006939.4(SOS2):c.3842A>G (p.Gln1281Arg)	SOS2 (Q1248R +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2710742	NM_006939.4(SOS2):c.3837T>C (p.Ser1279=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 1936984	NM_006939.4(SOS2):c.3832A>G (p.Ser1278Gly)	SOS2 (S1278G +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 475757	NM_006939.4(SOS2):c.3830T>C (p.Leu1277Pro)	SOS2 (L1277P)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +3 more	GBenign/Likely benign
Select item 996268	NM_006939.4(SOS2):c.3825T>C (p.Tyr1275=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9 +2 more	GLikely benign
Select item 512472	NM_006939.4(SOS2):c.3824A>G (p.Tyr1275Cys)	SOS2 (Y1275C)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GLikely benign
Select item 968756	NM_006939.4(SOS2):c.3818G>A (p.Arg1273Gln)	SOS2 (R1273Q)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GConflicting classifications of pathogenicity
Select item 2161879	NM_006939.4(SOS2):c.3817C>T (p.Arg1273Ter)	SOS2 (R1273* +1 more)	Single nucleotide variant (nonsense)	Noonan syndrome 9	GUncertain significance
Select item 1525148	NM_006939.4(SOS2):c.3815G>A (p.Arg1272His)	SOS2 (R1272H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 1443246	NM_006939.4(SOS2):c.3814C>T (p.Arg1272Cys)	SOS2 (R1272C)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1399673	NM_006939.4(SOS2):c.3814C>A (p.Arg1272Ser)	SOS2 (R1272S)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2721319	NM_006939.4(SOS2):c.3813G>T (p.Pro1271=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9 +1 more	GLikely benign
Select item 1541019	NM_006939.4(SOS2):c.3813G>C (p.Pro1271=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 384711	NM_006939.4(SOS2):c.3813G>A (p.Pro1271=)	SOS2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 2163879	NM_006939.4(SOS2):c.3812C>T (p.Pro1271Leu)	SOS2 (P1238L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2128727	NM_006939.4(SOS2):c.3810A>G (p.Val1270=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 2055059	NM_006939.4(SOS2):c.3808G>A (p.Val1270Ile)	SOS2 (V1237I +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2962548	NM_006939.4(SOS2):c.3800C>T (p.Ser1267Phe)	SOS2 (S1267F +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1541317	NM_006939.4(SOS2):c.3798C>G (p.Pro1266=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 1426213	NM_006939.4(SOS2):c.3797C>T (p.Pro1266Leu)	SOS2 (P1266L)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1349967	NM_006939.4(SOS2):c.3794C>T (p.Thr1265Ile)	SOS2 (T1265I)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1424003	NM_006939.4(SOS2):c.3793A>G (p.Thr1265Ala)	SOS2 (T1265A)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 984502	NM_006939.4(SOS2):c.3788C>G (p.Pro1263Arg)	SOS2 (P1263R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 1415196	NM_006939.4(SOS2):c.3785C>T (p.Pro1262Leu)	SOS2 (P1262L)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1471150	NM_006939.4(SOS2):c.3782C>G (p.Thr1261Ser)	SOS2 (T1261S)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GConflicting classifications of pathogenicity
Select item 475756	NM_006939.4(SOS2):c.3781A>C (p.Thr1261Pro)	SOS2 (T1261P)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2106362	NM_006939.4(SOS2):c.3779G>A (p.Ser1260Asn)	SOS2 (S1260N +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 717994	NM_006939.4(SOS2):c.3774G>A (p.Ser1258=)	SOS2	Single nucleotide variant (synonymous variant)	not specified +3 more	GLikely benign
Select item 2629044	NM_006939.4(SOS2):c.3773C>T (p.Ser1258Leu)	SOS2 (S1225L +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GConflicting classifications of pathogenicity
Select item 1362777	NM_006939.4(SOS2):c.3772T>G (p.Ser1258Ala)	SOS2 (S1258A)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 542399	NM_006939.4(SOS2):c.3769A>G (p.Asn1257Asp)	SOS2 (N1257D)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +2 more	GLikely benign
Select item 2845550	NM_006939.4(SOS2):c.3767C>A (p.Pro1256Gln)	SOS2 (P1223Q +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 718837	NM_006939.4(SOS2):c.3762G>A (p.Thr1254=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9 +1 more	GLikely benign
Select item 2084826	NM_006939.4(SOS2):c.3761C>T (p.Thr1254Met)	SOS2 (T1221M +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 542403	NM_006939.4(SOS2):c.3761C>G (p.Thr1254Arg)	SOS2 (T1254R)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2718524	NM_006939.4(SOS2):c.3758G>A (p.Ser1253Asn)	SOS2 (S1220N +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GLikely benign
Select item 962676	NM_006939.4(SOS2):c.3758G>C (p.Ser1253Thr)	SOS2 (S1253T)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 445735	NM_006939.4(SOS2):c.3755_3757del (p.Ile1252del)	SOS2 (I1252del)	Deletion (inframe_deletion)	RASopathy	GBenignFDA Recognized database
Select item 2147320	NM_006939.4(SOS2):c.3756T>G (p.Ile1252Met)	SOS2 (I1252M +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2752477	NM_006939.4(SOS2):c.3747C>T (p.Leu1249=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 475755	NM_006939.4(SOS2):c.3744G>T (p.Trp1248Cys)	SOS2 (W1248C)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +4 more	GBenign/Likely benign
Select item 855855	NM_006939.4(SOS2):c.3741C>G (p.Asp1247Glu)	SOS2 (D1247E)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1554467	NM_006939.4(SOS2):c.3738A>C (p.Ser1246=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 1367776	NM_006939.4(SOS2):c.3735T>G (p.Asp1245Glu)	SOS2 (D1245E)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 703832	NM_006939.4(SOS2):c.3729C>T (p.His1243=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9 +1 more	GLikely benign
Select item 2792309	NM_006939.4(SOS2):c.3721C>T (p.His1241Tyr)	SOS2 (H1208Y +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1931321	NM_006939.4(SOS2):c.3719G>C (p.Gly1240Ala)	SOS2 (G1240A +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2042481	NM_006939.4(SOS2):c.3714A>T (p.Pro1238=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 2188413	NM_006939.4(SOS2):c.3708A>G (p.Pro1236=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 1384708	NM_006939.4(SOS2):c.3707C>T (p.Pro1236Leu)	SOS2 (P1236L)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2085469	NM_006939.4(SOS2):c.3700C>G (p.Leu1234Val)	SOS2 (L1201V +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1504724	NM_006939.4(SOS2):c.3698A>C (p.Asn1233Thr)	SOS2 (N1233T)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +2 more	GConflicting classifications of pathogenicity
Select item 2122307	NM_006939.4(SOS2):c.3637_3693dup (p.Pro1231_Phe1232insProAspThrProProProValProLeuArgProProGluHisPheIleAsnCysPro)	SOS2	Duplication (inframe_insertion)	Noonan syndrome 9	GUncertain significance
Select item 2045849	NM_006939.4(SOS2):c.3684A>T (p.Ile1228=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 2021349	NM_006939.4(SOS2):c.3682A>G (p.Ile1228Val)	SOS2 (I1195V +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GLikely benign
Select item 2966007	NM_006939.4(SOS2):c.3681T>A (p.Phe1227Leu)	SOS2 (F1227L +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2917818	NM_006939.4(SOS2):c.3681T>C (p.Phe1227=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 1666158	NM_006939.4(SOS2):c.3681T>G (p.Phe1227Leu)	SOS2 (F1227L)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GLikely benign
Select item 2719822	NM_006939.4(SOS2):c.3677A>G (p.His1226Arg)	SOS2 (H1193R +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 1355420	NM_006939.4(SOS2):c.3673G>C (p.Glu1225Gln)	SOS2 (E1225Q)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity
Select item 2839137	NM_006939.4(SOS2):c.3672A>C (p.Pro1224=)	SOS2	Single nucleotide variant (synonymous variant)	Noonan syndrome 9	GLikely benign
Select item 1413186	NM_006939.4(SOS2):c.3671C>T (p.Pro1224Leu)	SOS2 (P1224L)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2759010	NM_006939.4(SOS2):c.3665G>C (p.Arg1222Pro)	SOS2 (R1189P +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9	GUncertain significance
Select item 2729109	NM_006939.4(SOS2):c.3665G>T (p.Arg1222Leu)	SOS2 (R1189L +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 2053953	NM_006939.4(SOS2):c.3664C>T (p.Arg1222Trp)	SOS2 (R1222W +1 more)	Single nucleotide variant (missense variant)	Noonan syndrome 9 +1 more	GUncertain significance

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