Favorite

Mutation Direct

Effortless mutation search and display tool

Search criteria：

Gene: DDHD2 & Disease: HSP, 158 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
39679	DDHD2	c.1978G>C	p.Asp660His (p.D660H)	NM_015214.3 M	SNV	P	3 +	4
	DDHD2	c.1978G>C	p.Asp660His (p.D660H)	NM_001164232.2	SNV	P	3 +	4
	DDHD2	c.1978G>C	p.Asp660His (p.D660H)	NM_001362911.2	SNV	P	3 +	4
	DDHD2	c.1978G>C	p.Asp660His (p.D660H)	NM_001362912.2	SNV	P	3 +	4
	DDHD2	c.1888G>C	p.Asp630His (p.D630H)	NM_001362913.2	SNV	P	3 +	4
	DDHD2	c.1978G>C	p.Asp660His (p.D660H)	NM_001362914.2	SNV	P	3 +	4
1344305	DDHD2	c.411+6C>T	--	NM_015214.3 M	SNV	VUS	2 +	2
935792	DDHD2	c.1720+6T>A	--	NM_015214.3 M	SNV	LB	2 +	2
1344305	DDHD2	c.411+6C>T	--	NM_001362914.2	SNV	VUS	2 +	2
	DDHD2	c.411+6C>T	--	NM_001362913.2	SNV	VUS	2 +	2
	DDHD2	c.411+6C>T	--	NM_001362912.2	SNV	VUS	2 +	2
	DDHD2	c.411+6C>T	--	NM_001362911.2	SNV	VUS	2 +	2
	DDHD2	c.411+6C>T	--	NM_001164234.2	SNV	VUS	2 +	2
	DDHD2	c.411+6C>T	--	NM_001164232.2	SNV	VUS	2 +	2
935792	DDHD2	c.1720+6T>A	--	NM_001362914.2	SNV	LB	2 +	2
	DDHD2	c.1630+6T>A	--	NM_001362913.2	SNV	LB	2 +	2
	DDHD2	c.1720+6T>A	--	NM_001362912.2	SNV	LB	2 +	2
	DDHD2	c.1720+6T>A	--	NM_001362911.2	SNV	LB	2 +	2
	DDHD2	c.1720+6T>A	--	NM_001164232.2	SNV	LB	2 +	2
697370	DDHD2	c.1386C>T	p.Asn462= (p.N462=)	NM_015214.3 M	SNV	LB	2 +	0

158 Results, 20 per Page

Comparison