Mad2l1bp Variant Search Result - Rat Genome Database

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26 records found for search term Mad2l1bp

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155939268	CV2225414	single nucleotide variant	NM_014628.3(MAD2L1BP):c.293A>G (p.Tyr98Cys)	not specified [RCV004100819]	uncertain significance	6	43636627	43636627	Human		name
155992250	CV2255798	single nucleotide variant	NM_014628.3(MAD2L1BP):c.182C>T (p.Pro61Leu)	not specified [RCV004120171]	uncertain significance	6	43636516	43636516	Human		name
156179992	CV2374721	single nucleotide variant	NM_014628.3(MAD2L1BP):c.124C>A (p.Pro42Thr)	not specified [RCV004225331]	uncertain significance	6	43636458	43636458	Human		name
407484864	CV3449500	single nucleotide variant	NM_014628.3(MAD2L1BP):c.226C>G (p.Leu76Val)	not specified [RCV004640443]	uncertain significance	6	43636560	43636560	Human		name
597646712	CV3693952	single nucleotide variant	NM_014628.3(MAD2L1BP):c.235C>T (p.His79Tyr)	not specified [RCV004942531]	uncertain significance	6	43636569	43636569	Human		name
597646726	CV3693954	single nucleotide variant	NM_014628.3(MAD2L1BP):c.149G>A (p.Cys50Tyr)	not specified [RCV004942533]	uncertain significance	6	43636483	43636483	Human		name
598183603	CV3992234	single nucleotide variant	NM_014628.3(MAD2L1BP):c.190G>A (p.Val64Met)	not specified [RCV005372956]	uncertain significance	6	43636524	43636524	Human		name
598164538	CV3992237	single nucleotide variant	NM_014628.3(MAD2L1BP):c.124C>G (p.Pro42Ala)	not specified [RCV005369021]	uncertain significance	6	43636458	43636458	Human		name
598164546	CV3992238	single nucleotide variant	NM_014628.3(MAD2L1BP):c.115A>G (p.Thr39Ala)	not specified [RCV005369022]	likely benign	6	43636449	43636449	Human		name
598183623	CV3992240	single nucleotide variant	NM_014628.3(MAD2L1BP):c.292T>C (p.Tyr98His)	not specified [RCV005372959]	uncertain significance	6	43636626	43636626	Human		name
156291278	CV2236425	single nucleotide variant	NM_014628.3(MAD2L1BP):c.545G>A (p.Ser182Asn)	not specified [RCV004108100]	uncertain significance	6	43640253	43640253	Human		name
156089950	CV2259156	single nucleotide variant	NM_014628.3(MAD2L1BP):c.818G>A (p.Arg273His)	not specified [RCV004120400]	likely benign	6	43640526	43640526	Human		name
156073628	CV2331598	single nucleotide variant	NM_014628.3(MAD2L1BP):c.443C>T (p.Pro148Leu)	not specified [RCV004184235]	uncertain significance	6	43640151	43640151	Human		name
155992767	CV2379348	single nucleotide variant	NM_014628.3(MAD2L1BP):c.340C>T (p.Arg114Trp)	not specified [RCV004223808]	uncertain significance	6	43640048	43640048	Human		name
156047007	CV2382395	single nucleotide variant	NM_014628.3(MAD2L1BP):c.613G>T (p.Ala205Ser)	not specified [RCV004230733]	uncertain significance	6	43640321	43640321	Human		name
401746951	CV2675295	single nucleotide variant	NM_014628.3(MAD2L1BP):c.731C>T (p.Thr244Ile)	not specified [RCV004290059]	uncertain significance	6	43640439	43640439	Human		name
405816293	CV3281248	single nucleotide variant	NM_014628.3(MAD2L1BP):c.709C>T (p.Arg237Trp)	not specified [RCV004411302]	uncertain significance	6	43640417	43640417	Human		name
405816294	CV3281249	single nucleotide variant	NM_014628.3(MAD2L1BP):c.800T>C (p.Val267Ala)	not specified [RCV004411303]	uncertain significance	6	43640508	43640508	Human		name
405816295	CV3281250	single nucleotide variant	NM_014628.3(MAD2L1BP):c.817C>T (p.Arg273Cys)	not specified [RCV004411304]	uncertain significance	6	43640525	43640525	Human		name
407484121	CV3449497	single nucleotide variant	NM_014628.3(MAD2L1BP):c.566G>A (p.Arg189His)	not specified [RCV004636377]	uncertain significance	6	43640274	43640274	Human		name
407484851	CV3449498	single nucleotide variant	NM_014628.3(MAD2L1BP):c.343G>A (p.Ala115Thr)	not specified [RCV004640441]	uncertain significance	6	43640051	43640051	Human		name
407484858	CV3449499	single nucleotide variant	NM_014628.3(MAD2L1BP):c.341G>A (p.Arg114Gln)	not specified [RCV004640442]	uncertain significance	6	43640049	43640049	Human		name
597646732	CV3693955	single nucleotide variant	NM_014628.3(MAD2L1BP):c.565C>T (p.Arg189Cys)	not specified [RCV004942534]	uncertain significance	6	43640273	43640273	Human		name
598183610	CV3992235	single nucleotide variant	NM_014628.3(MAD2L1BP):c.611A>C (p.Gln204Pro)	not specified [RCV005372957]	uncertain significance	6	43640319	43640319	Human		name
598183617	CV3992236	single nucleotide variant	NM_014628.3(MAD2L1BP):c.698G>A (p.Arg233Gln)	not specified [RCV005372958]	uncertain significance	6	43640406	43640406	Human		name
15182761	CV722051	single nucleotide variant	NM_014628.3(MAD2L1BP):c.590C>T (p.Ala197Val)	not provided [RCV000886068]	benign	6	43640298	43640298	Human		name

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