Stmn3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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14 records found for search term Stmn3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405741899	CV3334634	single nucleotide variant	NM_015894.4(STMN3):c.15T>G (p.Ile5Met)	not specified [RCV004465847]	uncertain significance	20	63653331	63653331	Human		name
329356377	CV2430720	single nucleotide variant	NM_015894.4(STMN3):c.58C>T (p.Leu20Phe)	not specified [RCV004253903]	uncertain significance	20	63644271	63644271	Human		name
155982356	CV2272960	single nucleotide variant	NM_015894.4(STMN3):c.175A>G (p.Lys59Glu)	not specified [RCV004135844]	uncertain significance	20	63643872	63643872	Human		name
155919987	CV2279520	single nucleotide variant	NM_015894.4(STMN3):c.152G>A (p.Gly51Asp)	not specified [RCV004142037]	uncertain significance	20	63643895	63643895	Human		name
156269898	CV2312063	single nucleotide variant	NM_015894.4(STMN3):c.249G>T (p.Glu83Asp)	not specified [RCV004164990]	uncertain significance	20	63643798	63643798	Human		name
401732741	CV2685320	single nucleotide variant	NM_015894.4(STMN3):c.182C>T (p.Pro61Leu)	not specified [RCV004292319]	uncertain significance	20	63643865	63643865	Human		name
597757877	CV3614962	single nucleotide variant	NM_015894.4(STMN3):c.143G>A (p.Arg48Gln)	not specified [RCV004868692]	uncertain significance	20	63643904	63643904	Human		name
155909213	CV2307232	single nucleotide variant	NM_015894.4(STMN3):c.467A>C (p.Glu156Ala)	not specified [RCV004159694]	uncertain significance	20	63642124	63642124	Human		name
329386244	CV2428227	single nucleotide variant	NM_015894.4(STMN3):c.457G>T (p.Ala153Ser)	not specified [RCV004251260]	uncertain significance	20	63642134	63642134	Human		name
329367556	CV2456915	single nucleotide variant	NM_015894.4(STMN3):c.530A>G (p.Glu177Gly)	not specified [RCV004270869]	uncertain significance	20	63641351	63641351	Human		name
405741906	CV3334635	single nucleotide variant	NM_015894.4(STMN3):c.452T>G (p.Leu151Arg)	not specified [RCV004465848]	uncertain significance	20	63642139	63642139	Human		name
598207902	CV3915901	single nucleotide variant	NM_015894.4(STMN3):c.334G>A (p.Glu112Lys)	not specified [RCV005291359]	uncertain significance	20	63642257	63642257	Human		name
598207908	CV3915902	single nucleotide variant	NM_015894.4(STMN3):c.478G>C (p.Glu160Gln)	not specified [RCV005291360]	uncertain significance	20	63642113	63642113	Human		name
598207915	CV3915903	single nucleotide variant	NM_015894.4(STMN3):c.348G>C (p.Glu116Asp)	not specified [RCV005291361]	uncertain significance	20	63642243	63642243	Human		name