HTR3E[gene] and "single gene"[properties] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2276252	NM_001256613.2(HTR3E):c.573G>C (p.Leu191Phe)	HTR3E (L206F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107571	NM_001256613.2(HTR3E):c.582G>A (p.Met194Ile)	HTR3E (M220I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382251	NM_001256613.2(HTR3E):c.610G>A (p.Ala204Thr)	HTR3E (A189T +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 721270	NM_001256613.2(HTR3E):c.617G>A (p.Arg206Gln)	HTR3E (R191Q +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2303073	NM_001256613.2(HTR3E):c.729C>G (p.Ile243Met)	HTR3E (I228M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107572	NM_001256613.2(HTR3E):c.745C>T (p.Leu249Phe)	HTR3E (L264F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521686	NM_001256613.2(HTR3E):c.749A>G (p.Tyr250Cys)	HTR3E (Y250C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507850	NM_001256613.2(HTR3E):c.759C>A (p.Asn253Lys)	HTR3E (N253K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107573	NM_001256613.2(HTR3E):c.794A>G (p.Asp265Gly)	HTR3E (D291G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107574	NM_001256613.2(HTR3E):c.817G>T (p.Val273Leu)	HTR3E (V258L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107575	NM_001256613.2(HTR3E):c.851C>T (p.Thr284Met)	HTR3E (T310M +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2533463	NM_001256613.2(HTR3E):c.937G>T (p.Ala313Ser)	HTR3E (A313S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493138	NM_001256613.2(HTR3E):c.958G>A (p.Val320Met)	HTR3E (V305M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107558	NM_001256613.2(HTR3E):c.977C>A (p.Thr326Asn)	HTR3E (T326N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588862	NM_001256613.2(HTR3E):c.977C>T (p.Thr326Ile)	HTR3E (T311I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224935	NM_001256613.2(HTR3E):c.1012A>C (p.Thr338Pro)	HTR3E (T364P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356187	NM_001256613.2(HTR3E):c.1033C>T (p.Arg345Trp)	HTR3E (R330W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393897	NM_001256613.2(HTR3E):c.1103A>G (p.Glu368Gly)	HTR3E (E368G +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2623234	NM_001256613.2(HTR3E):c.1112G>A (p.Gly371Asp)	HTR3E (G356D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107560	NM_001256613.2(HTR3E):c.1120C>G (p.Leu374Val)	HTR3E (L374V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107561	NM_001256613.2(HTR3E):c.1151A>G (p.Glu384Gly)	HTR3E (E399G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539973	NM_001256613.2(HTR3E):c.1216T>C (p.Trp406Arg)	HTR3E (W391R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319526	NM_001256613.2(HTR3E):c.1255C>A (p.His419Asn)	HTR3E (H404N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107562	NM_001256613.2(HTR3E):c.1259C>T (p.Ser420Leu)	HTR3E (S405L +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 713089	NM_001256613.2(HTR3E):c.1273T>G (p.Leu425Val)	HTR3E (L440V +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3107563	NM_001256613.2(HTR3E):c.1289C>T (p.Ala430Val)	HTR3E (A445V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272488	NM_001256613.2(HTR3E):c.1291A>G (p.Met431Val)	HTR3E (M431V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107564	NM_001256613.2(HTR3E):c.1300A>C (p.Met434Leu)	HTR3E (M419L +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3107565	NM_001256613.2(HTR3E):c.1309C>T (p.Arg437Cys)	HTR3E (R437C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458756	NM_001256613.2(HTR3E):c.1310G>A (p.Arg437His)	HTR3E (R452H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107566	NM_001256613.2(HTR3E):c.1348G>A (p.Val450Ile)	HTR3E (V435I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31