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Gene: TUB & Disease: RDOB, 47 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
956702	TUB	c.1232T>A	p.Leu411Gln (p.L411Q)	NM_177972.3 M	SNV	VUS	1 +	2
956724	TUB	c.1210C>T	p.Arg404Cys (p.R404C)	NM_177972.3 M	SNV	VUS	1 +	2
1170215	TUB	c.565+16A>G	--	NM_177972.3 M	SNV	B	1 +	2
1020820	TUB	c.451G>A	p.Val151Met (p.V151M)	NM_177972.3 M	SNV	VUS	1 +	2
804249	TUB	c.1215+1G>A	--	NM_177972.3 M	SNV	P	1 +	2
962044	TUB	c.364G>A	p.Ala122Thr (p.A122T)	NM_177972.3 M	SNV	VUS	1 +	2
954012	TUB	c.1270G>A	p.Glu424Lys (p.E424K)	NM_177972.3 M	SNV	VUS	1 +	2
1169389	TUB	c.360T>C	p.Gly120= (p.G120=)	NM_177972.3 M	SNV	B	1 +	2
956702	TUB	c.1397T>A	p.Leu466Gln (p.L466Q)	NM_003320.5	SNV	VUS	1 +	2
956724	TUB	c.1375C>T	p.Arg459Cys (p.R459C)	NM_003320.5	SNV	VUS	1 +	2
1170215	TUB	c.730+16A>G	--	NM_003320.5	SNV	B	1 +	2
1020820	TUB	c.616G>A	p.Val206Met (p.V206M)	NM_003320.5	SNV	VUS	1 +	2
804249	TUB	c.1380+1G>A	--	NM_003320.5	SNV	P	1 +	2
962044	TUB	c.529G>A	p.Ala177Thr (p.A177T)	NM_003320.5	SNV	VUS	1 +	2
954012	TUB	c.1435G>A	p.Glu479Lys (p.E479K)	NM_003320.5	SNV	VUS	1 +	2
1169389	TUB	c.525T>C	p.Gly175= (p.G175=)	NM_003320.5	SNV	B	1 +	2
162490	TUB	c.1194_1195del	p.Arg398fs (p.R398fs)	NM_177972.3 M	MS	P	1 +	1
1010424	TUB	c.1159G>A	p.Val387Met (p.V387M)	NM_177972.3 M	SNV	VUS	1 +	1
1684222	TUB	c.397+26C>G	--	NM_177972.3 M	SNV	B	1 +	1
1684224	TUB	c.566-47C>G	--	NM_177972.3 M	SNV	B	1 +	1

47 Results, 20 per Page

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