Smug1 Variant Search Result - Rat Genome Database

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26 records found for search term Smug1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
9686991	CV171523	single nucleotide variant	NM_001243787.2(SMUG1):c.285+5A>T	Prostate cancer [RCV000149210]	uncertain significance	12	54183651	54183651	Human	2	name
401775961	CV2692551	single nucleotide variant	NM_001243787.2(SMUG1):c.23G>A (p.Gly8Glu)	not specified [RCV004312294]	uncertain significance	12	54183918	54183918	Human		name
401885791	CV2783388	single nucleotide variant	NM_001243787.2(SMUG1):c.25T>C (p.Ser9Pro)	not specified [RCV004365741]	likely benign	12	54183916	54183916	Human		name
597727496	CV3597339	single nucleotide variant	NM_001243787.2(SMUG1):c.40G>A (p.Ala14Thr)	not specified [RCV004862687]	uncertain significance	12	54183901	54183901	Human		name
15199565	CV702398	single nucleotide variant	NM_001243787.2(SMUG1):c.44G>T (p.Gly15Val)	not provided [RCV000957074]	benign	12	54183897	54183897	Human		name
156154899	CV2266107	single nucleotide variant	NM_001243787.2(SMUG1):c.105G>T (p.Glu35Asp)	not specified [RCV004128701]	uncertain significance	12	54183836	54183836	Human		name
156256483	CV2369147	single nucleotide variant	NM_001243787.2(SMUG1):c.196C>T (p.Arg66Cys)	not specified [RCV004208072]	uncertain significance	12	54183745	54183745	Human		name
156267969	CV2398393	single nucleotide variant	NM_001243787.2(SMUG1):c.256C>G (p.Pro86Ala)	not specified [RCV004237728]	uncertain significance	12	54183685	54183685	Human		name
405713479	CV3325999	single nucleotide variant	NM_001243787.2(SMUG1):c.143C>T (p.Ser48Leu)	not specified [RCV004462142]	uncertain significance	12	54183798	54183798	Human		name
405713485	CV3326000	single nucleotide variant	NM_001243787.2(SMUG1):c.212G>A (p.Arg71His)	not specified [RCV004462143]	uncertain significance	12	54183729	54183729	Human		name
405713492	CV3326001	single nucleotide variant	NM_001243787.2(SMUG1):c.215A>G (p.Tyr72Cys)	not specified [RCV004462144]	uncertain significance	12	54183726	54183726	Human		name
597744349	CV3597338	single nucleotide variant	NM_001243787.2(SMUG1):c.197G>A (p.Arg66His)	not specified [RCV004865448]	uncertain significance	12	54183744	54183744	Human		name
598238296	CV3915262	single nucleotide variant	NM_001243787.2(SMUG1):c.250A>G (p.Met84Val)	not specified [RCV005275808]	uncertain significance	12	54183691	54183691	Human		name
156325788	CV2205434	single nucleotide variant	NM_001243787.2(SMUG1):c.360G>C (p.Glu120Asp)	not specified [RCV004082379]	uncertain significance	12	54182549	54182549	Human		name
155924338	CV2211523	single nucleotide variant	NM_001243787.2(SMUG1):c.730A>G (p.Asn244Asp)	not specified [RCV004084430]	uncertain significance	12	54182179	54182179	Human		name
156119723	CV2219292	single nucleotide variant	NM_001243787.2(SMUG1):c.415G>T (p.Ala139Ser)	not specified [RCV004095161]	uncertain significance	12	54182494	54182494	Human		name
156063716	CV2315978	single nucleotide variant	NM_001243787.2(SMUG1):c.638T>C (p.Val213Ala)	not specified [RCV004172043]	uncertain significance	12	54182271	54182271	Human		name
156278922	CV2325151	single nucleotide variant	NM_001243787.2(SMUG1):c.623G>A (p.Arg208Gln)	not specified [RCV004177575]	uncertain significance	12	54182286	54182286	Human		name
401863264	CV2776845	single nucleotide variant	NM_001243787.2(SMUG1):c.647T>C (p.Leu216Pro)	not specified [RCV004351675]	uncertain significance	12	54182262	54182262	Human		name
405713506	CV3326003	single nucleotide variant	NM_001243787.2(SMUG1):c.526A>G (p.Asn176Asp)	not specified [RCV004462146]	uncertain significance	12	54182383	54182383	Human		name
405713512	CV3326004	single nucleotide variant	NM_001243787.2(SMUG1):c.705A>C (p.Glu235Asp)	not specified [RCV004462147]	uncertain significance	12	54182204	54182204	Human		name
407452491	CV3474510	single nucleotide variant	NM_001243787.2(SMUG1):c.457G>A (p.Glu153Lys)	not specified [RCV004684071]	uncertain significance	12	54182452	54182452	Human		name
407503412	CV3474511	single nucleotide variant	NM_001243787.2(SMUG1):c.788G>T (p.Gly263Val)	not specified [RCV004670235]	uncertain significance	12	54182121	54182121	Human		name
597744354	CV3597340	single nucleotide variant	NM_001243787.2(SMUG1):c.524G>T (p.Arg175Leu)	not specified [RCV004865449]	uncertain significance	12	54182385	54182385	Human		name
598170594	CV3915261	single nucleotide variant	NM_001243787.2(SMUG1):c.629T>A (p.Val210Glu)	not specified [RCV005284637]	uncertain significance	12	54182280	54182280	Human		name
598170599	CV3915263	single nucleotide variant	NM_001243787.2(SMUG1):c.410G>C (p.Ser137Thr)	not specified [RCV005284638]	uncertain significance	12	54182499	54182499	Human		name

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