Related gene-specific medical variations for Gene (Select 259292) - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3324492	NM_176887.2(TAS2R46):c.845G>T (p.Gly282Val)	PRH1, PRH1-PRR4 +2 more (G282V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324491	NM_176887.2(TAS2R46):c.922T>C (p.Ser308Pro)	PRH1, PRH1-PRR4 +2 more (S308P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324490	NM_176887.2(TAS2R46):c.110A>G (p.Lys37Arg)	PRH1, PRH1-PRR4 +2 more (K37R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324489	NM_176887.2(TAS2R46):c.98T>C (p.Ile33Thr)	PRH1, PRH1-PRR4 +2 more (I33T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324488	NM_176887.2(TAS2R46):c.292C>T (p.Leu98Phe)	PRH1, PRH1-PRR4 +2 more (L98F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174116	NM_176887.2(TAS2R46):c.85T>A (p.Leu29Met)	PRH1, PRH1-PRR4 +2 more (L29M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174115	NM_176887.2(TAS2R46):c.802G>C (p.Ala268Pro)	PRH1, PRH1-PRR4 +2 more (A268P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174114	NM_176887.2(TAS2R46):c.265G>A (p.Ala89Thr)	PRH1, PRH1-PRR4 +2 more (A89T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3174113	NM_176887.2(TAS2R46):c.170G>A (p.Gly57Asp)	PRH1, PRH1-PRR4 +2 more (G57D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174112	NM_176887.2(TAS2R46):c.138A>C (p.Gln46His)	PRH1, PRH1-PRR4 +2 more (Q46H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3174111	NM_176887.2(TAS2R46):c.12T>G (p.Phe4Leu)	PRH1, PRH1-PRR4 +2 more (F4L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2642705	NM_176887.2(TAS2R46):c.24T>A (p.Ile8=)	PRH1, PRH1-PRR4 +2 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2642704	NM_176887.2(TAS2R46):c.54G>T (p.Val18=)	PRH1, PRH1-PRR4 +2 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2642703	NM_176887.2(TAS2R46):c.84A>G (p.Ala28=)	PRH1, PRH1-PRR4 +2 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2642702	NM_176887.2(TAS2R46):c.99T>C (p.Ile33=)	PRH1, PRH1-PRR4 +2 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2599418	NM_176887.2(TAS2R46):c.698C>T (p.Ser233Phe)	PRH1, PRH1-PRR4 +2 more (S233F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2568275	NM_176887.2(TAS2R46):c.914A>G (p.Lys305Arg)	PRH1, PRH1-PRR4 +2 more (K305R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395923	NM_176887.2(TAS2R46):c.821C>T (p.Thr274Ile)	PRH1, PRH1-PRR4 +2 more (T274I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395790	NM_176887.2(TAS2R46):c.70A>C (p.Asn24His)	PRH1, PRH1-PRR4 +2 more (N24H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359901	NM_176887.2(TAS2R46):c.410T>C (p.Leu137Ser)	PRH1, PRH1-PRR4 +2 more (L137S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349244	NM_176887.2(TAS2R46):c.894G>T (p.Arg298Ser)	PRH1, PRH1-PRR4 +2 more (R298S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330102	NM_176887.2(TAS2R46):c.694A>T (p.Thr232Ser)	PRH1, PRH1-PRR4 +2 more (T232S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301988	NM_176887.2(TAS2R46):c.271A>G (p.Ile91Val)	PRH1, PRH1-PRR4 +2 more (I91V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297826	NM_176887.2(TAS2R46):c.499A>C (p.Lys167Gln)	PRH1, PRH1-PRR4 +2 more (K167Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2287796	NM_176887.2(TAS2R46):c.647C>T (p.Ser216Phe)	PRH1, PRH1-PRR4 +2 more (S216F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2274325	NM_176887.2(TAS2R46):c.312A>G (p.Ile104Met)	PRH1, PRH1-PRR4 +2 more (I104M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2268146	NM_176887.2(TAS2R46):c.86T>C (p.Leu29Ser)	PRH1-PRR4, PRH1-TAS2R14 +2 more (L29S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260734	NM_176887.2(TAS2R46):c.814C>A (p.Pro272Thr)	PRH1, PRH1-PRR4 +2 more (P272T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250596	NM_176887.2(TAS2R46):c.507G>T (p.Arg169Ser)	PRH1, PRH1-PRR4 +2 more (R169S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2247247	NM_176887.2(TAS2R46):c.301A>G (p.Ser101Gly)	PRH1, PRH1-PRR4 +2 more (S101G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 30