Related gene-specific medical variations for Gene (Select 50840) - ClinVar

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Links from Gene

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3324466	NM_023922.2(TAS2R14):c.436G>A (p.Ala146Thr)	PRH1, PRH1-PRR4 +2 more (A146T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324465	NM_023922.2(TAS2R14):c.389T>G (p.Val130Gly)	PRH1, PRH1-PRR4 +2 more (V130G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324464	NM_023922.2(TAS2R14):c.658G>A (p.Gly220Arg)	PRH1, PRH1-PRR4 +2 more (G220R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3174042	NM_023922.2(TAS2R14):c.928C>T (p.His310Tyr)	PRH1, PRH1-PRR4 +2 more (H310Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174041	NM_023922.2(TAS2R14):c.833G>A (p.Cys278Tyr)	PRH1, PRH1-PRR4 +2 more (C137Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174040	NM_023922.2(TAS2R14):c.697G>A (p.Val233Met)	PRH1, PRH1-PRR4 +2 more (V233M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174039	NM_023922.2(TAS2R14):c.641A>G (p.His214Arg)	PRH1, PRH1-PRR4 +2 more (H214R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174038	NM_023922.2(TAS2R14):c.625C>G (p.Arg209Gly)	PRH1, PRH1-PRR4 +2 more (R209G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174036	NM_023922.2(TAS2R14):c.260A>G (p.Asn87Ser)	PRH1, PRH1-PRR4 +2 more (N87S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613025	NM_023922.2(TAS2R14):c.356T>G (p.Phe119Cys)	PRH1, PRH1-PRR4 +2 more (F119C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2612767	NM_023922.2(TAS2R14):c.454A>C (p.Ile152Leu)	PRH1, PRH1-PRR4 +2 more (I152L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601889	NM_023922.2(TAS2R14):c.790C>G (p.Leu264Val)	PRH1, PRH1-PRR4 +2 more (L264V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541093	NM_023922.2(TAS2R14):c.197G>T (p.Trp66Leu)	PRH1, PRH1-PRR4 +2 more (W66L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477614	NM_023922.2(TAS2R14):c.163C>G (p.Arg55Gly)	PRH1, PRH1-PRR4 +2 more (R55G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402539	NM_023922.2(TAS2R14):c.271G>A (p.Val91Met)	PRH1, PRH1-PRR4 +2 more (V91M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397247	NM_023922.2(TAS2R14):c.880G>C (p.Val294Leu)	PRH1, PRH1-PRR4 +2 more (V153L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344445	NM_023922.2(TAS2R14):c.164G>A (p.Arg55Gln)	TAS2R14, PRH1-TAS2R14 +2 more (R55Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299913	NM_023922.2(TAS2R14):c.463A>T (p.Ser155Cys)	PRH1, PRH1-PRR4 +2 more (S155C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293076	NM_023922.2(TAS2R14):c.248G>A (p.Arg83Lys)	PRH1, PRH1-PRR4 +2 more (R83K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292296	NM_023922.2(TAS2R14):c.614T>C (p.Met205Thr)	PRH1, PRH1-PRR4 +2 more (M205T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270715	NM_023922.2(TAS2R14):c.432T>A (p.Asn144Lys)	PRH1, PRH1-PRR4 +2 more (N144K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 791051	NM_023922.2(TAS2R14):c.609C>T (p.Phe203=)	PRH1, PRH1-PRR4 +2 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 740458	NM_023922.2(TAS2R14):c.87G>A (p.Leu29=)	PRH1, PRH1-PRR4 +2 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 719366	NM_023922.2(TAS2R14):c.189C>T (p.Phe63=)	PRH1-PRR4, PRH1-TAS2R14 +2 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 717257	NM_023922.2(TAS2R14):c.15A>G (p.Ile5Met)	PRH1, PRH1-PRR4 +2 more (I5M)	Single nucleotide variant (intron variant +1 more)	not provided	GBenign

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Links from Gene

Items: 25