Mln Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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51 records found for search term Mln

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597636680	CV3557227	single nucleotide variant	NM_002418.3(MLN):c.26C>T (p.Ala9Val)	not specified [RCV004824580]	uncertain significance	6	33801138	33801138	Human		name
156335226	CV2211436	single nucleotide variant	NM_002418.3(MLN):c.79G>A (p.Val27Ile)	not specified [RCV004090666]	uncertain significance	6	33801085	33801085	Human		name
155905090	CV2349677	single nucleotide variant	NM_002418.3(MLN):c.43G>A (p.Val15Ile)	not specified [RCV004204093]	uncertain significance	6	33801121	33801121	Human		name
329388951	CV2448531	single nucleotide variant	NM_002418.3(MLN):c.202C>A (p.Pro68Thr)	not specified [RCV004259214]	uncertain significance	6	33799137	33799137	Human		name
405759288	CV3364143	single nucleotide variant	NM_002418.3(MLN):c.224A>G (p.Glu75Gly)	not specified [RCV004500344]	uncertain significance	6	33799115	33799115	Human		name
597641773	CV3557225	single nucleotide variant	NM_002418.3(MLN):c.236T>C (p.Leu79Pro)	not specified [RCV004825517]	uncertain significance	6	33795604	33795604	Human		name
597641779	CV3557226	single nucleotide variant	NM_002418.3(MLN):c.260T>G (p.Met87Arg)	not specified [RCV004825518]	uncertain significance	6	33795580	33795580	Human		name
598167029	CV3989516	single nucleotide variant	NM_002418.3(MLN):c.127C>T (p.Arg43Trp)	not specified [RCV005369441]	uncertain significance	6	33799212	33799212	Human		name
8632022	CV87228	single nucleotide variant	NM_001040109.1(MLN):c.267G>A (p.Met89Ile)	Malignant melanoma [RCV000067319]	not provided	6	33795573	33795573	Human		name
156310734	CV2260083	single nucleotide variant	NM_001507.1(MLNR):c.4G>T (p.Gly2Cys)	not specified [RCV004119088]	uncertain significance	13	49220341	49220341	Human		name
156175817	CV2299706	single nucleotide variant	NM_001507.1(MLNR):c.19G>C (p.Gly7Arg)	not specified [RCV004148873]	uncertain significance	13	49220356	49220356	Human		name
597641798	CV3557230	single nucleotide variant	NM_001507.1(MLNR):c.23G>T (p.Ser8Ile)	not specified [RCV004825521]	uncertain significance	13	49220360	49220360	Human		name
401751764	CV2727134	single nucleotide variant	NM_001507.1(MLNR):c.49C>T (p.Pro17Ser)	not specified [RCV004325493]	uncertain significance	13	49220386	49220386	Human		name
401929800	CV2813901	single nucleotide variant	NM_001507.1(MLNR):c.981G>A (p.Ser327=)	not provided [RCV003390372]	likely benign	13	49222119	49222119	Human		name
405787907	CV3371606	single nucleotide variant	NM_001507.1(MLNR):c.92C>T (p.Ser31Leu)	not specified [RCV004505201]	uncertain significance	13	49220429	49220429	Human		name
407518744	CV3457440	single nucleotide variant	NM_001507.1(MLNR):c.44G>C (p.Arg15Pro)	not specified [RCV004628975]	uncertain significance	13	49220381	49220381	Human		name
407487281	CV3457441	single nucleotide variant	NM_001507.1(MLNR):c.79G>C (p.Glu27Gln)	not specified [RCV004641031]	uncertain significance	13	49220416	49220416	Human		name
156260757	CV2395573	single nucleotide variant	NM_001507.1(MLNR):c.268G>C (p.Gly90Arg)	not specified [RCV004241426]	uncertain significance	13	49220605	49220605	Human		name
329399591	CV2470193	single nucleotide variant	NM_001507.1(MLNR):c.199C>T (p.Arg67Trp)	not specified [RCV004287432]	uncertain significance	13	49220536	49220536	Human		name
401871906	CV2783631	single nucleotide variant	NM_001507.1(MLNR):c.256C>T (p.Leu86Phe)	not specified [RCV004365945]	uncertain significance	13	49220593	49220593	Human		name
156064548	CV2240237	single nucleotide variant	NM_001507.1(MLNR):c.695G>C (p.Ser232Thr)	not specified [RCV004112806]	uncertain significance	13	49221032	49221032	Human		name
156308765	CV2249556	single nucleotide variant	NM_001507.1(MLNR):c.604C>T (p.Leu202Phe)	not specified [RCV004120584]	uncertain significance	13	49220941	49220941	Human		name
156202720	CV2300662	single nucleotide variant	NM_001507.1(MLNR):c.831C>G (p.Ser277Arg)	not specified [RCV004155608]	uncertain significance	13	49221168	49221168	Human		name
156049984	CV2304546	single nucleotide variant	NM_001507.1(MLNR):c.911T>C (p.Val304Ala)	not specified [RCV004164624]	uncertain significance	13	49222049	49222049	Human		name
156186232	CV2324715	single nucleotide variant	NM_001507.1(MLNR):c.667G>C (p.Glu223Gln)	not specified [RCV004172954]	uncertain significance	13	49221004	49221004	Human		name
156191834	CV2335936	single nucleotide variant	NM_001507.1(MLNR):c.887C>T (p.Thr296Ile)	not specified [RCV004189547]	uncertain significance	13	49221224	49221224	Human		name
155902578	CV2356482	single nucleotide variant	NM_001507.1(MLNR):c.304C>T (p.Arg102Trp)	not specified [RCV004199399]	uncertain significance	13	49220641	49220641	Human		name
329401407	CV2460877	single nucleotide variant	NM_001507.1(MLNR):c.368A>C (p.Tyr123Ser)	not specified [RCV004271182]	uncertain significance	13	49220705	49220705	Human		name
401737788	CV2703647	single nucleotide variant	NM_001507.1(MLNR):c.611C>G (p.Ser204Trp)	not specified [RCV004315909]	uncertain significance	13	49220948	49220948	Human		name
401888724	CV2754856	single nucleotide variant	NM_001507.1(MLNR):c.334C>G (p.Arg112Gly)	not specified [RCV004341331]	uncertain significance	13	49220671	49220671	Human		name
401891084	CV2778633	single nucleotide variant	NM_001507.1(MLNR):c.828C>G (p.Ser276Arg)	not specified [RCV004344278]	likely benign	13	49221165	49221165	Human		name
401898486	CV2787759	single nucleotide variant	NM_001507.1(MLNR):c.307C>T (p.Pro103Ser)	not specified [RCV004356667]	uncertain significance	13	49220644	49220644	Human		name
405787789	CV3371586	single nucleotide variant	NM_001507.1(MLNR):c.928T>C (p.Cys310Arg)	not specified [RCV004505181]	uncertain significance	13	49222066	49222066	Human		name
405773999	CV3374744	single nucleotide variant	NM_001507.1(MLNR):c.406C>A (p.Arg136Ser)	not specified [RCV004502803]	uncertain significance	13	49220743	49220743	Human		name
405774185	CV3374776	single nucleotide variant	NM_001507.1(MLNR):c.424C>T (p.Arg142Cys)	not specified [RCV004502835]	uncertain significance	13	49220761	49220761	Human		name
405774740	CV3374842	single nucleotide variant	NM_001507.1(MLNR):c.562G>A (p.Val188Ile)	not specified [RCV004502901]	uncertain significance	13	49220899	49220899	Human		name
405786442	CV3374868	single nucleotide variant	NM_001507.1(MLNR):c.563T>C (p.Val188Ala)	not specified [RCV004504907]	uncertain significance	13	49220900	49220900	Human		name
405787075	CV3374969	single nucleotide variant	NM_001507.1(MLNR):c.686C>T (p.Ala229Val)	not specified [RCV004505008]	uncertain significance	13	49221023	49221023	Human		name
405786984	CV3374994	single nucleotide variant	NM_001507.1(MLNR):c.710C>G (p.Pro237Arg)	not specified [RCV004505033]	uncertain significance	13	49221047	49221047	Human		name
407487277	CV3457439	single nucleotide variant	NM_001507.1(MLNR):c.874G>A (p.Gly292Ser)	not specified [RCV004641030]	uncertain significance	13	49221211	49221211	Human		name
407487286	CV3457442	single nucleotide variant	NM_001507.1(MLNR):c.407G>T (p.Arg136Leu)	not specified [RCV004641032]	uncertain significance	13	49220744	49220744	Human		name
597641786	CV3557228	single nucleotide variant	NM_001507.1(MLNR):c.433C>A (p.Arg145Ser)	not specified [RCV004825519]	uncertain significance	13	49220770	49220770	Human		name
598188315	CV3989517	single nucleotide variant	NM_001507.1(MLNR):c.386T>G (p.Met129Arg)	not specified [RCV005373697]	uncertain significance	13	49220723	49220723	Human		name
598188321	CV3989518	single nucleotide variant	NM_001507.1(MLNR):c.707G>C (p.Arg236Pro)	not specified [RCV005373698]	uncertain significance	13	49221044	49221044	Human		name
598188327	CV3989519	single nucleotide variant	NM_001507.1(MLNR):c.706C>T (p.Arg236Trp)	not specified [RCV005373699]	uncertain significance	13	49221043	49221043	Human		name
155922537	CV2218978	single nucleotide variant	NM_001507.1(MLNR):c.1216G>A (p.Ala406Thr)	not specified [RCV004087159]	uncertain significance	13	49222354	49222354	Human		name
155918028	CV2283468	single nucleotide variant	NM_001507.1(MLNR):c.1151G>A (p.Arg384Lys)	not specified [RCV004139686]	uncertain significance	13	49222289	49222289	Human		name
401777010	CV2721568	single nucleotide variant	NM_001507.1(MLNR):c.1090G>C (p.Ala364Pro)	not specified [RCV004316079]	uncertain significance	13	49222228	49222228	Human		name
401882702	CV2774811	single nucleotide variant	NM_001507.1(MLNR):c.1048A>G (p.Ile350Val)	not specified [RCV004343903]	uncertain significance	13	49222186	49222186	Human		name
407487290	CV3457443	single nucleotide variant	NM_001507.1(MLNR):c.1072A>T (p.Ile358Phe)	not specified [RCV004641033]	uncertain significance	13	49222210	49222210	Human		name
597641791	CV3557229	single nucleotide variant	NM_001507.1(MLNR):c.1105C>A (p.Leu369Met)	not specified [RCV004825520]	uncertain significance	13	49222243	49222243	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

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InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

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