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Mutation Direct

Effortless mutation search and display tool

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Gene: TAS2R38 & Disease: THIOT, 3 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
2904	TAS2R38	c.145G>C	p.Ala49Pro (p.A49P)	NM_176817.5 M	SNV	VUS	1 +	1
2905	TAS2R38	c.785=	p.Ala262= (p.A262=)	NM_176817.5 M	SNV	B	1 +	1
2906	TAS2R38	c.886A>G	p.Ile296Val (p.I296V)	NM_176817.5 M	SNV	VUS	1 +	1

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