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Mutation Direct

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Gene: CTNNB1 & Disease: ST12, 96 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
17588	CTNNB1	c.134C>T	p.Ser45Phe (p.S45F)	NM_001904.4 M	SNV	P	11 +	11
17589	CTNNB1	c.133T>C	p.Ser45Pro (p.S45P)	NM_001904.4 M	SNV	P	8 +	11
17588	CTNNB1	c.134C>T	p.Ser45Phe (p.S45F)	NM_001098209.2	SNV	P	11 +	11
	CTNNB1	c.134C>T	p.Ser45Phe (p.S45F)	NM_001098210.2	SNV	P	11 +	11
	CTNNB1	c.113C>T	p.Ser38Phe (p.S38F)	NM_001330729.2	SNV	P	11 +	11
17589	CTNNB1	c.133T>C	p.Ser45Pro (p.S45P)	NM_001098209.2	SNV	P	8 +	11
	CTNNB1	c.133T>C	p.Ser45Pro (p.S45P)	NM_001098210.2	SNV	P	8 +	11
	CTNNB1	c.112T>C	p.Ser38Pro (p.S38P)	NM_001330729.2	SNV	P	8 +	11
17586	CTNNB1	c.110C>T	p.Ser37Phe (p.S37F)	NM_001904.4 M	SNV	P	12 +	10
	CTNNB1	c.110C>T	p.Ser37Phe (p.S37F)	NM_001098209.2	SNV	P	12 +	10
	CTNNB1	c.110C>T	p.Ser37Phe (p.S37F)	NM_001098210.2	SNV	P	12 +	10
	CTNNB1	c.89C>T	p.Ser30Phe (p.S30F)	NM_001330729.2	SNV	P	12 +	10
375895	CTNNB1	c.134C>A	p.Ser45Tyr (p.S45Y)	NM_001904.4 M	SNV	P	8 +	9
375894	CTNNB1	c.110C>A	p.Ser37Tyr (p.S37Y)	NM_001904.4 M	SNV	P	11 +	9
375895	CTNNB1	c.134C>A	p.Ser45Tyr (p.S45Y)	NM_001098209.2	SNV	P	8 +	9
	CTNNB1	c.134C>A	p.Ser45Tyr (p.S45Y)	NM_001098210.2	SNV	P	8 +	9
	CTNNB1	c.113C>A	p.Ser38Tyr (p.S38Y)	NM_001330729.2	SNV	P	8 +	9
375894	CTNNB1	c.110C>A	p.Ser37Tyr (p.S37Y)	NM_001098209.2	SNV	P	11 +	9
	CTNNB1	c.110C>A	p.Ser37Tyr (p.S37Y)	NM_001098210.2	SNV	P	11 +	9
	CTNNB1	c.89C>A	p.Ser30Tyr (p.S30Y)	NM_001330729.2	SNV	P	11 +	9

96 Results, 20 per Page

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