Cabp1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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11 records found for search term Cabp1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8653602	CV130177	single nucleotide variant	NM_001033677.1(CABP1):c.1087+931C>T	Lung cancer [RCV000110664]	uncertain significance	12	120662149	120662149	Human		name
8653603	CV130178	single nucleotide variant	NM_001033677.1(CABP1):c.1088-2227C>T	Lung cancer [RCV000110665]	uncertain significance	12	120664648	120664648	Human		name
156180678	CV2331473	single nucleotide variant	NM_001033677.2(CABP1):c.127A>T (p.Thr43Ser)	not specified [RCV004184105]	uncertain significance	12	120640812	120640812	Human		name
156184359	CV2349923	single nucleotide variant	NM_001033677.2(CABP1):c.274C>T (p.Arg92Trp)	not specified [RCV004206336]	uncertain significance	12	120640959	120640959	Human		name
156252388	CV2232398	single nucleotide variant	NM_001033677.2(CABP1):c.536T>G (p.Leu179Arg)	not specified [RCV004099025]	uncertain significance	12	120641221	120641221	Human		name
156257105	CV2369301	single nucleotide variant	NM_001033677.2(CABP1):c.852T>A (p.Asp284Glu)	not specified [RCV004208213]	uncertain significance	12	120660753	120660753	Human		name
156108397	CV2390234	single nucleotide variant	NM_001033677.2(CABP1):c.991A>C (p.Met331Leu)	not specified [RCV004240612]	uncertain significance	12	120661122	120661122	Human		name
401773535	CV2695276	single nucleotide variant	NM_001033677.2(CABP1):c.935G>A (p.Arg312Gln)	not specified [RCV004303405]	uncertain significance	12	120660836	120660836	Human		name
401719948	CV2705584	single nucleotide variant	NM_001033677.2(CABP1):c.839A>G (p.His280Arg)	not specified [RCV004318448]	uncertain significance	12	120660740	120660740	Human		name
597750391	CV3640755	single nucleotide variant	NM_001033677.2(CABP1):c.892A>G (p.Thr298Ala)	not specified [RCV004892574]	uncertain significance	12	120660793	120660793	Human		name
597762615	CV3640756	single nucleotide variant	NM_001033677.2(CABP1):c.874C>A (p.Pro292Thr)	not specified [RCV004895187]	uncertain significance	12	120660775	120660775	Human		name