ClinVar Miner

List of variants reported as benign for Noonan syndrome

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Total variants: 36
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HGVS dbSNP
NM_001354689.3(RAF1):c.1168+9_1168+21del rs727504451
NM_002755.4(MAP2K1):c.1068+12_1068+15del rs397516788
NM_002834.3:c.1-140delG
NM_002834.5(PTPN11):c.137+35G>A rs727505387
NM_002834.5(PTPN11):c.14+25G>C rs7972574
NM_002834.5(PTPN11):c.14+54C>A rs7973432
NM_002834.5(PTPN11):c.15-38C>T rs727505378
NM_002834.5(PTPN11):c.1599+26G>A rs727505390
NM_002834.5(PTPN11):c.1599+33A>G rs727505380
NM_002834.5(PTPN11):c.1600-95C>T rs3741983
NM_002834.5(PTPN11):c.255C>T (p.His85=) rs61736914
NM_002834.5(PTPN11):c.525+12G>C rs41304351
NM_002834.5(PTPN11):c.526-8C>A rs184804143
NM_002834.5(PTPN11):c.757-69T>C rs150087259
NM_002834.5(PTPN11):c.854-21C>T rs41279090
NM_002834.5(PTPN11):c.854-30T>C rs144391508
NM_002834.5(PTPN11):c.854-32A>C rs187389813
NM_002834.5(PTPN11):c.925A>G (p.Ile309Val) rs201787206
NM_005633.3:c.213+15C>G
NM_005633.4(SOS1):c.1074+5G>C rs145155424
NM_005633.4(SOS1):c.1203-20T>C rs112906251
NM_005633.4(SOS1):c.1230G>A (p.Gln410=) rs141390073
NM_005633.4(SOS1):c.195A>C (p.Arg65=) rs7609455
NM_005633.4(SOS1):c.2371C>A (p.Leu791Ile) rs142004123
NM_005633.4(SOS1):c.2791+53C>T rs7577088
NM_005633.4(SOS1):c.2964+32T>G rs727505384
NM_005633.4(SOS1):c.3081+26G>A rs186106971
NM_005633.4(SOS1):c.3081+32A>G rs6723430
NM_005633.4(SOS1):c.3347-20T>G rs727505382
NM_005633.4(SOS1):c.720+25C>G rs997344
NM_006270.5(RRAS):c.243C>T (p.Ile81=) rs116683551
NM_006270.5(RRAS):c.333C>T (p.Asn111=) rs1865077
NM_006270.5(RRAS):c.397G>A (p.Asp133Asn) rs61760904
NM_006270.5(RRAS):c.408C>T (p.Pro136=) rs114187560
NM_006270.5(RRAS):c.454-10C>G rs731861
NM_006270.5(RRAS):c.54A>T (p.Gly18=) rs571103858

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