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Gene: HNRNPH1 & Disease: Bain Type of X-Linked Syndromic Intellectual Disability, 33 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count
828178	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001257293.2 M	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364225.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364228.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364229.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364230.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364231.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364232.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364233.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364234.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364235.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364236.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364237.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364238.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364239.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364240.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364241.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364242.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364226.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001364227.2	SNV	LP	2 +
	HNRNPH1	c.340C>T	p.Arg114Trp (p.R114W)	NM_001363572.2	SNV	LP	2 +

33 Results, 20 per Page

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