Favorite

Mutation Direct

Effortless mutation search and display tool

Search criteria：

Gene: PROM1 & Disease: RP41, 351 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
5610	PROM1	c.1117C>T	p.Arg373Cys (p.R373C)	NM_006017.3 M	SNV	P	9 +	18
	PROM1	c.1090C>T	p.Arg364Cys (p.R364C)	NM_001145847.2	SNV	P	9 +	18
	PROM1	c.1090C>T	p.Arg364Cys (p.R364C)	NM_001145848.2	SNV	P	9 +	18
	PROM1	c.1117C>T	p.Arg373Cys (p.R373C)	NM_001145849.2	SNV	P	9 +	18
	PROM1	c.1117C>T	p.Arg373Cys (p.R373C)	NM_001145850.2	SNV	P	9 +	18
	PROM1	c.1090C>T	p.Arg364Cys (p.R364C)	NM_001145851.2	SNV	P	9 +	18
	PROM1	c.1090C>T	p.Arg364Cys (p.R364C)	NM_001145852.2	SNV	P	9 +	18
	PROM1	c.1090C>T	p.Arg364Cys (p.R364C)	NM_001371406.1	SNV	P	9 +	18
	PROM1	c.1090C>T	p.Arg364Cys (p.R364C)	NM_001371407.1	SNV	P	9 +	18
	PROM1	c.1090C>T	p.Arg364Cys (p.R364C)	NM_001371408.1	SNV	P	9 +	18
372711	PROM1	c.1354dupT	--	NM_006017.3 M	Dup	P	7 +	11
	PROM1	c.1354dup	p.Tyr452fs (p.Y452fs)	NM_006017.3 M	Dup	P	7 +	11
	PROM1	c.1327dup	p.Tyr443fs (p.Y443fs)	NM_001145847.2	Dup	P	7 +	11
	PROM1	c.1327dup	p.Tyr443fs (p.Y443fs)	NM_001145848.2	Dup	P	7 +	11
	PROM1	c.1354dup	p.Tyr452fs (p.Y452fs)	NM_001145849.2	Dup	P	7 +	11
	PROM1	c.1354dup	p.Tyr452fs (p.Y452fs)	NM_001145850.2	Dup	P	7 +	11
	PROM1	c.1327dup	p.Tyr443fs (p.Y443fs)	NM_001145851.2	Dup	P	7 +	11
	PROM1	c.1327dup	p.Tyr443fs (p.Y443fs)	NM_001145852.2	Dup	P	7 +	11
	PROM1	c.1327dup	p.Tyr443fs (p.Y443fs)	NM_001371406.1	Dup	P	7 +	11
	PROM1	c.1327dup	p.Tyr443fs (p.Y443fs)	NM_001371407.1	Dup	P	7 +	11

351 Results, 20 per Page

...

Comparison