Hint2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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18 records found for search term Hint2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329395816	CV2454625	single nucleotide variant	NM_032593.3(HINT2):c.11C>T (p.Ala4Val)	not specified [RCV004268085]	likely benign	9	35814969	35814969	Human		name
405778467	CV3270265	single nucleotide variant	NM_032593.3(HINT2):c.11C>G (p.Ala4Gly)	not specified [RCV004397183]	uncertain significance	9	35814969	35814969	Human		name
597762199	CV3685901	single nucleotide variant	NM_032593.3(HINT2):c.17T>G (p.Val6Gly)	not specified [RCV004926076]	uncertain significance	9	35814963	35814963	Human		name
401767995	CV2727347	single nucleotide variant	NM_032593.3(HINT2):c.73G>A (p.Gly25Arg)	not specified [RCV004327452]	uncertain significance	9	35814907	35814907	Human		name
329376986	CV2435768	single nucleotide variant	NM_032593.3(HINT2):c.173G>A (p.Arg58Gln)	not specified [RCV004253396]	uncertain significance	9	35813693	35813693	Human		name
401768609	CV2716671	single nucleotide variant	NM_032593.3(HINT2):c.104C>T (p.Thr35Ile)	not specified [RCV004327727]	uncertain significance	9	35813762	35813762	Human		name
405778473	CV3270266	single nucleotide variant	NM_032593.3(HINT2):c.166T>A (p.Phe56Ile)	not specified [RCV004397184]	uncertain significance	9	35813700	35813700	Human		name
405778477	CV3270267	single nucleotide variant	NM_032593.3(HINT2):c.248C>T (p.Pro83Leu)	not specified [RCV004397185]	uncertain significance	9	35813524	35813524	Human		name
407527134	CV3437333	single nucleotide variant	NM_032593.3(HINT2):c.296G>A (p.Arg99Gln)	not specified [RCV004632693]	uncertain significance	9	35813476	35813476	Human		name
329399450	CV2470103	single nucleotide variant	NM_032593.3(HINT2):c.310G>A (p.Glu104Lys)	not specified [RCV004287361]	uncertain significance	9	35813462	35813462	Human		name
401763746	CV2704128	single nucleotide variant	NM_032593.3(HINT2):c.407A>G (p.Asn136Ser)	not specified [RCV004308992]	uncertain significance	9	35813139	35813139	Human		name
405778483	CV3270268	single nucleotide variant	NM_032593.3(HINT2):c.318A>C (p.Glu106Asp)	not specified [RCV004397186]	likely benign	9	35813454	35813454	Human		name
407527137	CV3437334	single nucleotide variant	NM_032593.3(HINT2):c.308C>A (p.Ala103Asp)	not specified [RCV004632694]	uncertain significance	9	35813464	35813464	Human		name
597762203	CV3685902	single nucleotide variant	NM_032593.3(HINT2):c.466C>G (p.Arg156Gly)	not specified [RCV004926077]	uncertain significance	9	35813080	35813080	Human		name
597762208	CV3685903	single nucleotide variant	NM_032593.3(HINT2):c.386A>T (p.Asp129Val)	not specified [RCV004926078]	uncertain significance	9	35813280	35813280	Human		name
597762213	CV3685904	single nucleotide variant	NM_032593.3(HINT2):c.466C>T (p.Arg156Trp)	not specified [RCV004926079]	uncertain significance	9	35813080	35813080	Human		name
597762218	CV3685905	single nucleotide variant	NM_032593.3(HINT2):c.464G>T (p.Gly155Val)	not specified [RCV004926080]	uncertain significance	9	35813082	35813082	Human		name
598177984	CV3978854	single nucleotide variant	NM_032593.3(HINT2):c.395G>A (p.Arg132Gln)	not specified [RCV005351922]	uncertain significance	9	35813271	35813271	Human		name