Related gene-specific medical variations for Gene (Select 285242) - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2512296	NM_001256613.2(HTR3E):c.368C>A (p.Pro123Gln)	HTR3E, HTR3E-AS1 (P108Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2512190	NM_001256613.2(HTR3E):c.184G>C (p.Val62Leu)	HTR3E, HTR3E-AS1 (V77L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2458174	NM_001256613.2(HTR3E):c.347C>T (p.Ala116Val)	HTR3E, HTR3E-AS1 (A101V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2240766	NM_001256613.2(HTR3E):c.401A>G (p.Asp134Gly)	HTR3E, HTR3E-AS1 (D149G +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2219550	NM_001256613.2(HTR3E):c.473T>C (p.Val158Ala)	HTR3E-AS1, HTR3E (V143A +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2217430	NM_001256613.2(HTR3E):c.358C>G (p.Leu120Val)	HTR3E-AS1, HTR3E (L105V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2205974	NM_001256613.2(HTR3E):c.332C>T (p.Thr111Met)	HTR3E, HTR3E-AS1 (T126M +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1242214	NM_001256613.2(HTR3E):c.211G>A (p.Ala71Thr)	HTR3E, HTR3E-AS1 (A71T +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign