Slc38a7 Variant Search Result - Rat Genome Database

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32 records found for search term Slc38a7

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598243650	CV3914958	single nucleotide variant	NM_018231.3(SLC38A7):c.71G>C (p.Arg24Pro)	not specified [RCV005276738]	uncertain significance	16	58680056	58680056	Human		name
15151967	CV726721	single nucleotide variant	NM_018231.3(SLC38A7):c.864C>T (p.Leu288=)	not provided [RCV000879709]	benign	16	58675959	58675959	Human		name
15150174	CV726722	single nucleotide variant	NM_018231.3(SLC38A7):c.29A>G (p.Tyr10Cys)	not provided [RCV000879321]	benign	16	58680098	58680098	Human		name
156311370	CV2260165	single nucleotide variant	NM_018231.3(SLC38A7):c.197G>T (p.Gly66Val)	not specified [RCV004119154]	uncertain significance	16	58679930	58679930	Human		name
329399699	CV2443436	single nucleotide variant	NM_018231.3(SLC38A7):c.178G>A (p.Val60Ile)	not specified [RCV004262276]	uncertain significance	16	58679949	58679949	Human		name
405708811	CV3329077	single nucleotide variant	NM_018231.3(SLC38A7):c.149C>T (p.Thr50Ile)	not specified [RCV004461465]	uncertain significance	16	58679978	58679978	Human		name
405708817	CV3329078	single nucleotide variant	NM_018231.3(SLC38A7):c.194T>G (p.Leu65Arg)	not specified [RCV004461466]	uncertain significance	16	58679933	58679933	Human		name
598243666	CV3914960	single nucleotide variant	NM_018231.3(SLC38A7):c.187G>A (p.Ala63Thr)	not specified [RCV005276740]	uncertain significance	16	58679940	58679940	Human		name
15163559	CV715003	single nucleotide variant	NM_018231.3(SLC38A7):c.1362C>T (p.Asn454=)	not provided [RCV000970510]	benign	16	58667412	58667412	Human		name
155901153	CV2294344	single nucleotide variant	NM_018231.3(SLC38A7):c.530A>G (p.Lys177Arg)	not specified [RCV004159870]	uncertain significance	16	58678414	58678414	Human		name
156142945	CV2296168	single nucleotide variant	NM_018231.3(SLC38A7):c.961G>A (p.Val321Met)	not specified [RCV004154089]	uncertain significance	16	58672166	58672166	Human		name
156068233	CV2320388	single nucleotide variant	NM_018231.3(SLC38A7):c.865G>A (p.Ala289Thr)	not specified [RCV004178547]	uncertain significance	16	58675958	58675958	Human		name
329402080	CV2453967	single nucleotide variant	NM_018231.3(SLC38A7):c.367T>C (p.Cys123Arg)	not specified [RCV004271636]	uncertain significance	16	58678798	58678798	Human		name
401724020	CV2684940	single nucleotide variant	NM_018231.3(SLC38A7):c.956T>C (p.Met319Thr)	not specified [RCV004296442]	uncertain significance	16	58672171	58672171	Human		name
401741846	CV2706425	single nucleotide variant	NM_018231.3(SLC38A7):c.499G>C (p.Gly167Arg)	not specified [RCV004317253]	uncertain significance	16	58678445	58678445	Human		name
401874857	CV2781306	single nucleotide variant	NM_018231.3(SLC38A7):c.847G>A (p.Ala283Thr)	not specified [RCV004352325]	uncertain significance	16	58675976	58675976	Human		name
405708821	CV3329079	single nucleotide variant	NM_018231.3(SLC38A7):c.317G>A (p.Cys106Tyr)	not specified [RCV004461467]	uncertain significance	16	58678848	58678848	Human		name
405708828	CV3329080	single nucleotide variant	NM_018231.3(SLC38A7):c.967G>A (p.Val323Ile)	not specified [RCV004461468]	uncertain significance	16	58672160	58672160	Human		name
407514714	CV3484563	single nucleotide variant	NM_018231.3(SLC38A7):c.412T>C (p.Tyr138His)	not specified [RCV004674670]	uncertain significance	16	58678753	58678753	Human		name
407451634	CV3484564	single nucleotide variant	NM_018231.3(SLC38A7):c.928G>A (p.Val310Met)	not specified [RCV004683726]	uncertain significance	16	58672199	58672199	Human		name
597765740	CV3599918	single nucleotide variant	NM_018231.3(SLC38A7):c.742A>G (p.Met248Val)	not specified [RCV004870483]	uncertain significance	16	58676315	58676315	Human		name
598243658	CV3914959	single nucleotide variant	NM_018231.3(SLC38A7):c.310G>T (p.Ala104Ser)	not specified [RCV005276739]	uncertain significance	16	58678855	58678855	Human		name
598237221	CV3914963	single nucleotide variant	NM_018231.3(SLC38A7):c.947C>T (p.Ser316Leu)	not specified [RCV005275614]	uncertain significance	16	58672180	58672180	Human		name
155916265	CV2239693	single nucleotide variant	NM_018231.3(SLC38A7):c.1174G>A (p.Gly392Ser)	not specified [RCV004108238]	uncertain significance	16	58671102	58671102	Human		name
156291171	CV2296608	single nucleotide variant	NM_018231.3(SLC38A7):c.1220T>C (p.Phe407Ser)	not specified [RCV004154669]	uncertain significance	16	58671056	58671056	Human		name
156185372	CV2377841	single nucleotide variant	NM_018231.3(SLC38A7):c.1207G>A (p.Ala403Thr)	not specified [RCV004230417]	uncertain significance	16	58671069	58671069	Human		name
329373619	CV2434553	single nucleotide variant	NM_018231.3(SLC38A7):c.1058G>A (p.Arg353His)	not specified [RCV004254254]	uncertain significance	16	58671218	58671218	Human		name
401879658	CV2769676	single nucleotide variant	NM_018231.3(SLC38A7):c.1378C>T (p.Leu460Phe)	not specified [RCV004351601]	uncertain significance	16	58667396	58667396	Human		name
405708798	CV3329075	single nucleotide variant	NM_018231.3(SLC38A7):c.1180G>T (p.Val394Leu)	not specified [RCV004461463]	uncertain significance	16	58671096	58671096	Human		name
405708803	CV3329076	single nucleotide variant	NM_018231.3(SLC38A7):c.1207G>T (p.Ala403Ser)	not specified [RCV004461464]	uncertain significance	16	58671069	58671069	Human		name
598243676	CV3914961	single nucleotide variant	NM_018231.3(SLC38A7):c.1364C>T (p.Ala455Val)	not specified [RCV005276741]	uncertain significance	16	58667410	58667410	Human		name
598243681	CV3914962	single nucleotide variant	NM_018231.3(SLC38A7):c.1065G>C (p.Gln355His)	not specified [RCV005276742]	uncertain significance	16	58671211	58671211	Human		name

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