"Ambry Genetics"[submitter] AND "HTR3C"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2206063	NM_130770.3(HTR3C):c.109C>A (p.Gln37Lys)	HTR3C, LOC126806891 (Q37K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329355	NM_130770.3(HTR3C):c.116G>C (p.Gly39Ala)	HTR3C, LOC126806891 (G39A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107535	NM_130770.3(HTR3C):c.123C>A (p.Asp41Glu)	HTR3C, LOC126806891 (D41E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107537	NM_130770.3(HTR3C):c.194G>A (p.Arg65His)	HTR3C (R65H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2481192	NM_130770.3(HTR3C):c.257C>T (p.Thr86Ile)	HTR3C (T86I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404754	NM_130770.3(HTR3C):c.407C>T (p.Thr136Met)	HTR3C (T136M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254351	NM_130770.3(HTR3C):c.503A>G (p.Tyr168Cys)	HTR3C (Y168C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107538	NM_130770.3(HTR3C):c.541A>G (p.Ser181Gly)	HTR3C (S181G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107539	NM_130770.3(HTR3C):c.556A>G (p.Thr186Ala)	HTR3C (T186A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538664	NM_130770.3(HTR3C):c.616C>T (p.Arg206Cys)	HTR3C (R206C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107540	NM_130770.3(HTR3C):c.617G>A (p.Arg206His)	HTR3C (R206H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3285045	NM_130770.3(HTR3C):c.725C>T (p.Ala242Val)	HTR3C (A242V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285043	NM_130770.3(HTR3C):c.733C>T (p.Arg245Cys)	HTR3C (R245C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107542	NM_130770.3(HTR3C):c.742A>G (p.Ser248Gly)	HTR3C (S248G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570380	NM_130770.3(HTR3C):c.833G>A (p.Arg278His)	HTR3C (R278H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2214591	NM_130770.3(HTR3C):c.842T>G (p.Phe281Cys)	HTR3C (F281C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353909	NM_130770.3(HTR3C):c.937G>A (p.Ala313Thr)	HTR3C (A313T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107543	NM_130770.3(HTR3C):c.947T>G (p.Leu316Arg)	HTR3C (L316R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403433	NM_130770.3(HTR3C):c.991T>C (p.Tyr331His)	HTR3C (Y331H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3107533	NM_130770.3(HTR3C):c.1003G>C (p.Val335Leu)	HTR3C (V335L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3107536	NM_130770.3(HTR3C):c.1243T>C (p.Trp415Arg)	HTR3C (W415R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285042	NM_130770.3(HTR3C):c.1283G>A (p.Arg428His)	HTR3C (R428H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 22