Birc5 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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23 records found for search term Birc5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401935886	CV2808448	single nucleotide variant	NM_001168.3(BIRC5):c.*50G>C	not provided [RCV003413350]	benign	17	78223604	78223604	Human		name
156151793	CV2245224	single nucleotide variant	NM_001168.3(BIRC5):c.222-671T>G	not specified [RCV004106996]	uncertain significance	17	78215993	78215993	Human		name
329397574	CV2456310	single nucleotide variant	NM_001168.3(BIRC5):c.222-664A>T	not specified [RCV004275478]	uncertain significance	17	78216000	78216000	Human		name
405867088	CV2842573	single nucleotide variant	NM_001168.3(BIRC5):c.222-639G>A	EBV-positive nodal T- and NK-cell lymphoma [RCV004557930]	likely benign	17	78216025	78216025	Human		name
405867067	CV2842583	single nucleotide variant	NM_001168.3(BIRC5):c.222-667A>C	EBV-positive nodal T- and NK-cell lymphoma [RCV004557940]	likely benign	17	78215997	78215997	Human		name
405263476	CV3185140	single nucleotide variant	NM_001168.3(BIRC5):c.340-638G>A	not provided [RCV003885704]	likely benign	17	78222827	78222827	Human		name
405730785	CV3294600	single nucleotide variant	NM_001168.3(BIRC5):c.222-682G>A	not specified [RCV004429314]	uncertain significance	17	78215982	78215982	Human		name
597715558	CV3636730	single nucleotide variant	NM_001168.3(BIRC5):c.222-682G>C	not specified [RCV004887209]	uncertain significance	17	78215982	78215982	Human		name
405730793	CV3294601	single nucleotide variant	NM_001168.3(BIRC5):c.23C>T (p.Pro8Leu)	not specified [RCV004429315]	uncertain significance	17	78214339	78214339	Human		name
401867100	CV2792605	single nucleotide variant	NM_001168.3(BIRC5):c.76C>A (p.Pro26Thr)	not specified [RCV004363629]	uncertain significance	17	78214392	78214392	Human		name
401914863	CV2808447	single nucleotide variant	NM_001168.3(BIRC5):c.315C>T (p.Asp105=)	not provided [RCV003428504]	likely benign	17	78216757	78216757	Human		name
598161484	CV3949532	single nucleotide variant	NM_001168.3(BIRC5):c.48C>G (p.Asp16Glu)	not specified [RCV005307016]	uncertain significance	17	78214364	78214364	Human		name
155932649	CV2364436	single nucleotide variant	NM_001168.3(BIRC5):c.242C>T (p.Ser81Leu)	not specified [RCV004223644]	uncertain significance	17	78216684	78216684	Human		name
156100036	CV2392913	single nucleotide variant	NM_001168.3(BIRC5):c.247G>A (p.Gly83Ser)	not specified [RCV004247262]	uncertain significance	17	78216689	78216689	Human		name
405730801	CV3294602	single nucleotide variant	NM_001168.3(BIRC5):c.253G>T (p.Ala85Ser)	not specified [RCV004429316]	uncertain significance	17	78216695	78216695	Human		name
155970690	CV2217871	single nucleotide variant	NM_001168.3(BIRC5):c.406G>A (p.Glu136Lys)	not specified [RCV004084040]	uncertain significance	17	78223531	78223531	Human		name
329387684	CV2446767	single nucleotide variant	NM_001168.3(BIRC5):c.397C>T (p.Arg133Cys)	not specified [RCV004257633]	likely benign	17	78223522	78223522	Human		name
401726122	CV2699103	single nucleotide variant	NM_001168.3(BIRC5):c.398G>A (p.Arg133His)	not specified [RCV004303613]	uncertain significance	17	78223523	78223523	Human		name
405730810	CV3294603	single nucleotide variant	NM_001168.3(BIRC5):c.355A>C (p.Asn119His)	not specified [RCV004429317]	uncertain significance	17	78223480	78223480	Human		name
405730819	CV3294604	single nucleotide variant	NM_001168.3(BIRC5):c.394C>T (p.Arg132Cys)	not specified [RCV004429318]	uncertain significance	17	78223519	78223519	Human		name
407473187	CV3427669	single nucleotide variant	NM_001168.3(BIRC5):c.395G>A (p.Arg132His)	not specified [RCV004600303]	uncertain significance	17	78223520	78223520	Human		name
597715567	CV3636731	single nucleotide variant	NM_001168.3(BIRC5):c.425A>C (p.Asp142Ala)	not specified [RCV004887210]	uncertain significance	17	78223550	78223550	Human		name
8636371	CV91594	single nucleotide variant	NM_001012271.1(BIRC5):c.76C>T (p.Pro26Ser)	Malignant melanoma [RCV000071692]	not provided	17	78214392	78214392	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)

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

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MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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