Cirbp Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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20 records found for search term Cirbp

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8636610	CV91835	single nucleotide variant	NM_001280.2(CIRBP):c.502+146C>G	Malignant melanoma [RCV000071933]	not provided	19	1272197	1272197	Human		name
15174399	CV731246	single nucleotide variant	NM_001300829.2(CIRBP):c.104-10C>T	not provided [RCV000884125]	benign	19	1271130	1271130	Human		name
8636609	CV91834	single nucleotide variant	NM_001280.2(CIRBP):c.269C>T (p.Ser90Phe)	Malignant melanoma [RCV000071932]	not provided	19	1271387	1271387	Human		name
15152535	CV741587	single nucleotide variant	NM_001300829.2(CIRBP):c.639C>G (p.Ser213=)	not provided [RCV000901585]	benign	19	1272188	1272188	Human		name
401876044	CV2777635	single nucleotide variant	NM_001300829.2(CIRBP):c.170T>C (p.Ile57Thr)	not specified [RCV004343477]	uncertain significance	19	1271206	1271206	Human		name
405683892	CV3293907	single nucleotide variant	NM_001300829.2(CIRBP):c.272G>A (p.Arg91His)	not specified [RCV004443967]	uncertain significance	19	1271390	1271390	Human		name
156175185	CV2278188	single nucleotide variant	NM_001300829.2(CIRBP):c.311T>A (p.Phe104Tyr)	not specified [RCV004141382]	uncertain significance	19	1271429	1271429	Human		name
155977022	CV2342843	single nucleotide variant	NM_001300829.2(CIRBP):c.397G>C (p.Gly133Arg)	not specified [RCV004189880]	uncertain significance	19	1271598	1271598	Human		name
329401617	CV2457223	single nucleotide variant	NM_001300829.2(CIRBP):c.347G>A (p.Arg116Lys)	not specified [RCV004265296]	uncertain significance	19	1271465	1271465	Human		name
401739806	CV2684178	single nucleotide variant	NM_001300829.2(CIRBP):c.469G>A (p.Gly157Ser)	not specified [RCV004288849]	uncertain significance	19	1272018	1272018	Human		name
401718266	CV2728506	single nucleotide variant	NM_001300829.2(CIRBP):c.344C>G (p.Ser115Cys)	not specified [RCV004333434]	uncertain significance	19	1271462	1271462	Human		name
405683897	CV3293908	single nucleotide variant	NM_001300829.2(CIRBP):c.335G>T (p.Arg112Leu)	not specified [RCV004443968]	uncertain significance	19	1271453	1271453	Human		name
597781418	CV3650386	single nucleotide variant	NM_001300829.2(CIRBP):c.368A>G (p.Tyr123Cys)	not specified [RCV004899777]	uncertain significance	19	1271569	1271569	Human		name
597781422	CV3650387	single nucleotide variant	NM_001300829.2(CIRBP):c.334C>T (p.Arg112Cys)	not specified [RCV004899778]	uncertain significance	19	1271452	1271452	Human		name
597781427	CV3650388	single nucleotide variant	NM_001300829.2(CIRBP):c.472G>A (p.Gly158Arg)	not specified [RCV004899779]	uncertain significance	19	1272021	1272021	Human		name
598231511	CV3948185	single nucleotide variant	NM_001300829.2(CIRBP):c.416G>C (p.Arg139Thr)	not specified [RCV005319565]	uncertain significance	19	1271617	1271617	Human		name
598231518	CV3948186	single nucleotide variant	NM_001300829.2(CIRBP):c.313C>T (p.Arg105Cys)	not specified [RCV005319566]	uncertain significance	19	1271431	1271431	Human		name
598231525	CV3948187	single nucleotide variant	NM_001300829.2(CIRBP):c.308T>G (p.Phe103Cys)	not specified [RCV005319567]	uncertain significance	19	1271426	1271426	Human		name
598231531	CV3948188	single nucleotide variant	NM_001300829.2(CIRBP):c.460C>T (p.Arg154Trp)	not specified [RCV005319568]	uncertain significance	19	1272009	1272009	Human		name
598231537	CV3948189	single nucleotide variant	NM_001300829.2(CIRBP):c.301C>T (p.Arg101Trp)	not specified [RCV005319569]	uncertain significance	19	1271419	1271419	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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