"Ambry Genetics"[submitter] AND "TAS2R31"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2462555	NM_176885.2(TAS2R31):c.926C>T (p.Pro309Leu)	PRH1, PRH1-PRR4 +2 more (P309L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174080	NM_176885.2(TAS2R31):c.856C>G (p.Leu286Val)	PRH1, PRH1-PRR4 +2 more (L286V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341075	NM_176885.2(TAS2R31):c.840T>G (p.Ile280Met)	PRH1, PRH1-PRR4 +2 more (I280M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257170	NM_176885.2(TAS2R31):c.826C>G (p.Pro276Ala)	PRH1, PRH1-PRR4 +2 more (P276A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2341314	NM_176885.2(TAS2R31):c.815C>T (p.Pro272Leu)	PRH1, PRH1-PRR4 +2 more (P272L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174079	NM_176885.2(TAS2R31):c.643G>A (p.Gly215Arg)	PRH1, PRH1-PRR4 +2 more (G215R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470478	NM_176885.2(TAS2R31):c.559C>T (p.Pro187Ser)	PRH1, PRH1-PRR4 +2 more (P187S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208677	NM_176885.2(TAS2R31):c.483C>A (p.Asn161Lys)	PRH1, PRH1-PRR4 +2 more (N161K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347037	NM_176885.2(TAS2R31):c.464C>A (p.Thr155Lys)	PRH1, PRH1-PRR4 +2 more (T155K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328059	NM_176885.2(TAS2R31):c.446T>C (p.Met149Thr)	PRH1, PRH1-PRR4 +2 more (M149T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369482	NM_176885.2(TAS2R31):c.334A>T (p.Asn112Tyr)	PRH1, PRH1-PRR4 +2 more (N112Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371226	NM_176885.2(TAS2R31):c.298A>G (p.Thr100Ala)	PRH1, PRH1-PRR4 +2 more (T100A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324470	NM_176885.2(TAS2R31):c.254A>G (p.Tyr85Cys)	PRH1, PRH1-PRR4 +2 more (Y85C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174076	NM_176885.2(TAS2R31):c.251C>T (p.Ala84Val)	PRH1, PRH1-PRR4 +2 more (A84V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2380867	NM_176885.2(TAS2R31):c.104G>A (p.Arg35Gln)	PRH1, PRH1-PRR4 +2 more (R35Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2600393	NM_176885.2(TAS2R31):c.56T>C (p.Ile19Thr)	PRH1, PRH1-PRR4 +2 more (I19T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358445	NM_176885.2(TAS2R31):c.40G>A (p.Val14Met)	PRH1, PRH1-PRR4 +2 more (V14M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174077	NM_176885.2(TAS2R31):c.37G>A (p.Val13Ile)	PRH1, PRH1-PRR4 +2 more (V13I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292026	NM_176885.2(TAS2R31):c.35T>A (p.Val12Glu)	PRH1, PRH1-PRR4 +2 more (V12E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance