"Ambry Genetics"[submitter] AND "TAS2R41"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2359248	NM_176883.2(TAS2R41):c.55C>G (p.Leu19Val)	EPHA1-AS1, TAS2R41 (L19V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355209	NM_176883.2(TAS2R41):c.56T>C (p.Leu19Pro)	EPHA1-AS1, TAS2R41 (L19P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2227088	NM_176883.2(TAS2R41):c.65C>T (p.Ala22Val)	TAS2R41, EPHA1-AS1 (A22V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2291015	NM_176883.2(TAS2R41):c.217A>G (p.Lys73Glu)	EPHA1-AS1, TAS2R41 (K73E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377886	NM_176883.2(TAS2R41):c.245G>A (p.Arg82Gln)	EPHA1-AS1, TAS2R41 (R82Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2511950	NM_176883.2(TAS2R41):c.413T>A (p.Val138Asp)	EPHA1-AS1, TAS2R41 (V138D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2557347	NM_176883.2(TAS2R41):c.575C>A (p.Pro192His)	EPHA1-AS1, TAS2R41 (P192H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2463260	NM_176883.2(TAS2R41):c.683C>A (p.Ala228Asp)	EPHA1-AS1, TAS2R41 (A228D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2329364	NM_176883.2(TAS2R41):c.713C>A (p.Ser238Tyr)	TAS2R41, EPHA1-AS1 (S238Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261033	NM_176883.2(TAS2R41):c.751A>C (p.Ile251Leu)	EPHA1-AS1, TAS2R41 (I251L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2302901	NM_176883.2(TAS2R41):c.787G>A (p.Asp263Asn)	EPHA1-AS1, TAS2R41 (D263N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2308240	NM_176883.2(TAS2R41):c.806A>G (p.Gln269Arg)	EPHA1-AS1, TAS2R41 (Q269R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2391874	NM_176883.2(TAS2R41):c.811G>A (p.Ala271Thr)	TAS2R41, EPHA1-AS1 (A271T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2480271	NM_176883.2(TAS2R41):c.853T>A (p.Phe285Ile)	TAS2R41, EPHA1-AS1 (F285I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance