SOS1[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59133	GRCh38/hg38 2p25.3-16.1(chr2:66097-55570637)x3	LOC129933242, LOC129933243 +1631 more	Copy number gain	See cases	GPathogenic
Select item 155615	GRCh38/hg38 2p25.3-21(chr2:236816-45983232)x3	ABCG5, ABCG8 +1400 more	Copy number gain	See cases	GPathogenic
Select item 152995	GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3	LOC129934199, LOC129934200 +2457 more	Copy number gain	See cases	GBenign
Select item 150617	GRCh38/hg38 2p22.2-21(chr2:37000557-41954686)x1	ARHGEF33, ATL2 +154 more	Copy number loss	See cases	GPathogenic
Select item 2650843	NM_001145451.5(ARHGEF33):c.2343+2156G>A	ARHGEF33, SOS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3025206	NM_001145451.5(ARHGEF33):c.2343+2201C>A	ARHGEF33, SOS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 335963	NM_005633.4(SOS1):c.*4265A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 335964	NM_005633.4(SOS1):c.*4221C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 335965	NM_005633.4(SOS1):c.*4110C>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 898505	NM_005633.4(SOS1):c.*4077G>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 898506	NM_005633.4(SOS1):c.*4076C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 335966	NM_005633.4(SOS1):c.*4023T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 895514	NM_005633.4(SOS1):c.*4014T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 895515	NM_005633.4(SOS1):c.*3989G>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 335967	NM_005633.4(SOS1):c.*3918T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GBenign
Select item 895516	NM_005633.4(SOS1):c.*3811T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 896917	NM_005633.4(SOS1):c.*3750T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 335968	NM_005633.4(SOS1):c.*3727G>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 335969	NM_005633.4(SOS1):c.*3725T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 335970	NM_005633.4(SOS1):c.*3724T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign
Select item 1701378	NM_005633.4(SOS1):c.*3718del	SOS1	Deletion (3 prime UTR variant)	not provided	GBenign
Select item 335971	NM_005633.4(SOS1):c.*3592C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 897416	NM_005633.4(SOS1):c.*3569T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +2 more	GBenign/Likely benign
Select item 335972	NM_005633.4(SOS1):c.3566_3568del	SOS1	Deletion (3 prime UTR variant)	Gingival fibromatosis +1 more	GUncertain significance
Select item 335973	NM_005633.4(SOS1):c.*3539T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 335974	NM_005633.4(SOS1):c.*3463A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 898584	NM_005633.4(SOS1):c.*3458A>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +2 more	GBenign/Likely benign
Select item 335975	NM_005633.4(SOS1):c.*3451A>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +2 more	GConflicting classifications of pathogenicity
Select item 335976	NM_005633.4(SOS1):c.3416_3417del	SOS1	Deletion (3 prime UTR variant)	Gingival fibromatosis +1 more	GUncertain significance
Select item 895589	NM_005633.4(SOS1):c.*3367G>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 895590	NM_005633.4(SOS1):c.*3326T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 895591	NM_005633.4(SOS1):c.*3291C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 895592	NM_005633.4(SOS1):c.*3252A>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 895593	NM_005633.4(SOS1):c.*3230T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 335977	NM_005633.4(SOS1):c.3189_3192del	SOS1	Deletion (3 prime UTR variant)	Gingival fibromatosis +2 more	GConflicting classifications of pathogenicity
Select item 896997	NM_005633.4(SOS1):c.*3158T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 896998	NM_005633.4(SOS1):c.*3149C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 896999	NM_005633.4(SOS1):c.*3041A>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 335978	NM_005633.4(SOS1):c.*2983C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 897478	NM_005633.4(SOS1):c.*2893C>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 897479	NM_005633.4(SOS1):c.*2662G>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 897480	NM_005633.4(SOS1):c.*2574A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 335979	NM_005633.4(SOS1):c.*2567T>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign
Select item 898636	NM_005633.4(SOS1):c.*2517C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign/Likely benign
Select item 898637	NM_005633.4(SOS1):c.*2512C>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 335980	NM_005633.4(SOS1):c.2503_2506dup	SOS1	Duplication (3 prime UTR variant)	Noonan syndrome +1 more	GUncertain significance
Select item 335981	NM_005633.4(SOS1):c.*2497G>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 335982	NM_005633.4(SOS1):c.*2439del	SOS1	Deletion (3 prime UTR variant)	Noonan syndrome +1 more	GLikely benign
Select item 895652	NM_005633.4(SOS1):c.*2257C>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 895653	NM_005633.4(SOS1):c.*2246A>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 212289	NM_005633.4(SOS1):c.2244_2245dup	SOS1	Duplication (3 prime UTR variant)	Gingival fibromatosis +4 more	GLikely benign
Select item 335983	NM_005633.4(SOS1):c.*2218T>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 335984	NM_005633.4(SOS1):c.*2208dup	SOS1	Duplication (3 prime UTR variant)	Noonan syndrome +1 more	GUncertain significance
Select item 895654	NM_005633.4(SOS1):c.*2160C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 897068	NM_005633.4(SOS1):c.*2138G>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 335985	NM_005633.4(SOS1):c.2063_2066dup	SOS1	Duplication (3 prime UTR variant)	Noonan syndrome +1 more	GUncertain significance
Select item 897069	NM_005633.4(SOS1):c.*2056A>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 335986	NM_005633.4(SOS1):c.2048_2050dup	SOS1	Duplication (3 prime UTR variant)	Gingival fibromatosis +1 more	GUncertain significance
Select item 897070	NM_005633.4(SOS1):c.*1998G>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 335987	NM_005633.4(SOS1):c.*1844A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign
Select item 897546	NM_005633.4(SOS1):c.*1762A>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 335988	NM_005633.4(SOS1):c.*1731A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 335989	NM_005633.4(SOS1):c.*1694del	SOS1	Deletion (3 prime UTR variant)	Gingival fibromatosis +4 more	GConflicting classifications of pathogenicity
Select item 335990	NM_005633.4(SOS1):c.*1684G>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 335991	NM_005633.4(SOS1):c.*1678C>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 1678394	NM_005633.4(SOS1):c.*1652A>T	SOS1	Single nucleotide variant (3 prime UTR variant)	not provided	GUncertain significance
Select item 898697	NM_005633.4(SOS1):c.*1641A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 212288	NM_005633.4(SOS1):c.*1606del	SOS1	Deletion (3 prime UTR variant)	Gingival fibromatosis +4 more	GLikely benign
Select item 335992	NM_005633.4(SOS1):c.*1589T>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 335993	NM_005633.4(SOS1):c.*1552T>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 895719	NM_005633.4(SOS1):c.*1535G>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 335994	NM_005633.4(SOS1):c.*1516G>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 895720	NM_005633.4(SOS1):c.*1477G>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 895721	NM_005633.4(SOS1):c.*1412A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 896004	NM_005633.4(SOS1):c.*1396G>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 896005	NM_005633.4(SOS1):c.*1391C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 335995	NM_005633.4(SOS1):c.*1385A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 335996	NM_005633.4(SOS1):c.1333_1336dup	SOS1	Duplication (3 prime UTR variant)	Noonan syndrome 4 +4 more	GBenign/Likely benign
Select item 335997	NM_005633.4(SOS1):c.*1309A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 335998	NM_005633.4(SOS1):c.*1303C>A	SOS1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 897600	NM_005633.4(SOS1):c.*1270T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 335999	NM_005633.4(SOS1):c.*1224A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 336000	NM_005633.4(SOS1):c.*1090TTTG[1]	SOS1	Microsatellite (3 prime UTR variant)	Gingival fibromatosis +1 more	GUncertain significance
Select item 897601	NM_005633.4(SOS1):c.*1085A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GBenign/Likely benign
Select item 898759	NM_005633.4(SOS1):c.*1049G>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 336001	NM_005633.4(SOS1):c.*909G>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 898760	NM_005633.4(SOS1):c.*873C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 336002	NM_005633.4(SOS1):c.*855G>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 336003	NM_005633.4(SOS1):c.*805C>A	SOS1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 336004	NM_005633.4(SOS1):c.*766del	SOS1	Deletion (3 prime UTR variant)	Noonan syndrome +1 more	GUncertain significance
Select item 336005	NM_005633.4(SOS1):c.*758A>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +2 more	GConflicting classifications of pathogenicity
Select item 336006	NM_005633.4(SOS1):c.*696G>A	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome +1 more	GUncertain significance
Select item 895788	NM_005633.4(SOS1):c.*664C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Fibromatosis, gingival, 1 +1 more	GUncertain significance
Select item 336007	NM_005633.4(SOS1):c.*642T>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 896074	NM_005633.4(SOS1):c.*559C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 336008	NM_005633.4(SOS1):c.*544C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 336009	NM_005633.4(SOS1):c.*534C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 896075	NM_005633.4(SOS1):c.*483A>C	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 897662	NM_005633.4(SOS1):c.*421A>G	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance
Select item 897663	NM_005633.4(SOS1):c.*408C>T	SOS1	Single nucleotide variant (3 prime UTR variant)	Noonan syndrome 4 +1 more	GUncertain significance

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