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Gene: HRAS & Disease: Noonan Syndrome and Noonan-Related Syndrome, 96 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
12602	HRAS	c.34G>A	p.Gly12Ser (p.G12S)	NM_005343.4 M	SNV	P	30 +	36
	HRAS	c.34G>A	p.Gly12Ser (p.G12S)	NM_001130442.3	SNV	P	30 +	36
	HRAS	c.-286G>A	--	NM_001318054.2	SNV	P	30 +	36
	HRAS	c.34G>A	p.Gly12Ser (p.G12S)	NM_176795.5	SNV	P	30 +	36
12603	HRAS	c.35G>C	p.Gly12Ala (p.G12A)	NM_005343.4 M	SNV	P	33 +	23
	HRAS	c.35G>C	p.Gly12Ala (p.G12A)	NM_001130442.3	SNV	P	33 +	23
	HRAS	c.-285G>C	--	NM_001318054.2	SNV	P	33 +	23
	HRAS	c.35G>C	p.Gly12Ala (p.G12A)	NM_176795.5	SNV	P	33 +	23
12612	HRAS	c.35G>A	p.Gly12Asp (p.G12D)	NM_005343.4 M	SNV	P	5 +	20
	HRAS	c.35G>A	p.Gly12Asp (p.G12D)	NM_001130442.3	SNV	P	5 +	20
	HRAS	c.-285G>A	--	NM_001318054.2	SNV	P	5 +	20
	HRAS	c.35G>A	p.Gly12Asp (p.G12D)	NM_176795.5	SNV	P	5 +	20
12606	HRAS	c.37G>T	p.Gly13Cys (p.G13C)	NM_005343.4 M	SNV	P	27 +	18
35554	HRAS	c.37G>C	p.Gly13Arg (p.G13R)	NM_005343.4 M	SNV	P	23 +	18
12606	HRAS	c.37G>T	p.Gly13Cys (p.G13C)	NM_001130442.3	SNV	P	27 +	18
	HRAS	c.-283G>T	--	NM_001318054.2	SNV	P	27 +	18
	HRAS	c.37G>T	p.Gly13Cys (p.G13C)	NM_176795.5	SNV	P	27 +	18
35554	HRAS	c.37G>C	p.Gly13Arg (p.G13R)	NM_001130442.3	SNV	P	23 +	18
	HRAS	c.-283G>C	--	NM_001318054.2	SNV	P	23 +	18
	HRAS	c.37G>C	p.Gly13Arg (p.G13R)	NM_176795.5	SNV	P	23 +	18

96 Results, 20 per Page

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