Ebna1bp2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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18 records found for search term Ebna1bp2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156099778	CV2306569	single nucleotide variant	NM_006824.3(EBNA1BP2):c.16C>G (p.Leu6Val)	not specified [RCV004157175]	uncertain significance	1	43172103	43172103	Human		name
401877403	CV2790157	single nucleotide variant	NM_006824.3(EBNA1BP2):c.73G>C (p.Asp25His)	not specified [RCV004364086]	uncertain significance	1	43171963	43171963	Human		name
597803022	CV3667202	single nucleotide variant	NM_006824.3(EBNA1BP2):c.32C>T (p.Ser11Leu)	not specified [RCV004907000]	uncertain significance	1	43172087	43172087	Human		name
155943750	CV2241739	single nucleotide variant	NM_001159936.1(EBNA1BP2):c.5A>G (p.Tyr2Cys)	not specified [RCV004106679]	uncertain significance	1	43172417	43172417	Human		name
401753033	CV2725069	single nucleotide variant	NM_006824.3(EBNA1BP2):c.127C>A (p.Pro43Thr)	not specified [RCV004319821]	uncertain significance	1	43171909	43171909	Human		name
597803020	CV3667201	single nucleotide variant	NM_006824.3(EBNA1BP2):c.131A>G (p.Lys44Arg)	not specified [RCV004906999]	uncertain significance	1	43171905	43171905	Human		name
15098006	CV696750	single nucleotide variant	NM_006824.3(EBNA1BP2):c.227C>G (p.Pro76Arg)	not provided [RCV000958452]	benign	1	43171575	43171575	Human		name
156090152	CV2206563	single nucleotide variant	NM_006824.3(EBNA1BP2):c.308A>C (p.Gln103Pro)	not specified [RCV004080911]	uncertain significance	1	43171494	43171494	Human		name
156369646	CV2263380	single nucleotide variant	NM_006824.3(EBNA1BP2):c.421G>A (p.Ala141Thr)	not specified [RCV004133642]	uncertain significance	1	43170782	43170782	Human		name
155915063	CV2264876	single nucleotide variant	NM_006824.3(EBNA1BP2):c.877C>T (p.Pro293Ser)	not specified [RCV004134628]	uncertain significance	1	43164487	43164487	Human		name
155931506	CV2293550	single nucleotide variant	NM_006824.3(EBNA1BP2):c.619T>C (p.Ser207Pro)	not specified [RCV004153077]	uncertain significance	1	43166914	43166914	Human		name
156122241	CV2354318	single nucleotide variant	NM_006824.3(EBNA1BP2):c.545C>T (p.Thr182Met)	not specified [RCV004206735]	uncertain significance	1	43167228	43167228	Human		name
401888125	CV2791264	single nucleotide variant	NM_006824.3(EBNA1BP2):c.375G>T (p.Gln125His)	not specified [RCV004356895]	uncertain significance	1	43170828	43170828	Human		name
405752881	CV3238382	single nucleotide variant	NM_006824.3(EBNA1BP2):c.452G>A (p.Arg151Gln)	not specified [RCV004382258]	uncertain significance	1	43169024	43169024	Human		name
407478283	CV3441441	single nucleotide variant	NM_006824.3(EBNA1BP2):c.785G>A (p.Arg262Gln)	not specified [RCV004617489]	uncertain significance	1	43164728	43164728	Human		name
407478289	CV3441442	single nucleotide variant	NM_006824.3(EBNA1BP2):c.335C>T (p.Ala112Val)	not specified [RCV004617490]	uncertain significance	1	43170868	43170868	Human		name
598268805	CV3953937	single nucleotide variant	NM_006824.3(EBNA1BP2):c.745G>T (p.Gly249Cys)	not specified [RCV005327178]	uncertain significance	1	43164768	43164768	Human		name
15169603	CV707415	single nucleotide variant	NM_006824.3(EBNA1BP2):c.869A>T (p.Asn290Ile)	not provided [RCV000971844]	benign	1	43164644	43164644	Human		name