Bmp10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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32 records found for search term Bmp10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8577394	CV111769	single nucleotide variant	NM_014482.1(BMP10):c.335-853G>A	Lung cancer [RCV000092292]	uncertain significance	2	68867424	68867424	Human		name
156332514	CV2220695	single nucleotide variant	NM_014482.3(BMP10):c.86A>C (p.Gln29Pro)	not specified [RCV004097869]	uncertain significance	2	68871273	68871273	Human		name
401727975	CV2678625	single nucleotide variant	NM_014482.3(BMP10):c.268A>G (p.Asn90Asp)	not specified [RCV004292626]	uncertain significance	2	68871091	68871091	Human		name
401730150	CV2700464	single nucleotide variant	NM_014482.3(BMP10):c.259G>A (p.Glu87Lys)	not specified [RCV004311101]	uncertain significance	2	68871100	68871100	Human		name
401778560	CV2709271	single nucleotide variant	NM_014482.3(BMP10):c.202C>T (p.Leu68Phe)	not specified [RCV004316432]	uncertain significance	2	68871157	68871157	Human		name
401737698	CV2718181	single nucleotide variant	NM_014482.3(BMP10):c.281C>G (p.Thr94Arg)	not specified [RCV004315879]	uncertain significance	2	68871078	68871078	Human		name
401887524	CV2771991	single nucleotide variant	NM_014482.3(BMP10):c.221A>G (p.Gln74Arg)	not specified [RCV004344674]	uncertain significance	2	68871138	68871138	Human		name
405749337	CV3291189	single nucleotide variant	NM_014482.3(BMP10):c.287G>A (p.Arg96Gln)	not specified [RCV004431859]	uncertain significance	2	68871072	68871072	Human		name
405749343	CV3291190	single nucleotide variant	NM_014482.3(BMP10):c.289A>T (p.Thr97Ser)	not specified [RCV004431860]	uncertain significance	2	68871070	68871070	Human		name
407473961	CV3423942	single nucleotide variant	NM_014482.3(BMP10):c.257T>G (p.Leu86Trp)	not specified [RCV004600494]	uncertain significance	2	68871102	68871102	Human		name
156192976	CV2301928	single nucleotide variant	NM_014482.3(BMP10):c.550C>A (p.Leu184Met)	not specified [RCV004156708]	uncertain significance	2	68866356	68866356	Human		name
156167206	CV2315287	single nucleotide variant	NM_014482.3(BMP10):c.652C>A (p.His218Asn)	not specified [RCV004167274]	uncertain significance	2	68866254	68866254	Human		name
156305550	CV2338834	single nucleotide variant	NM_014482.3(BMP10):c.991G>A (p.Asp331Asn)	not specified [RCV004182389]	uncertain significance	2	68865915	68865915	Human		name
329357164	CV2457568	single nucleotide variant	NM_014482.3(BMP10):c.737A>G (p.Gln246Arg)	not specified [RCV004269158]	likely benign	2	68866169	68866169	Human		name
401721054	CV2702245	single nucleotide variant	NM_014482.3(BMP10):c.566G>C (p.Gly189Ala)	not specified [RCV004314583]	uncertain significance	2	68866340	68866340	Human		name
401772499	CV2719660	single nucleotide variant	NM_014482.3(BMP10):c.667C>T (p.His223Tyr)	not specified [RCV004329107]	uncertain significance	2	68866239	68866239	Human		name
401757511	CV2735059	single nucleotide variant	NM_014482.3(BMP10):c.487C>T (p.Arg163Trp)	not specified [RCV004333757]	uncertain significance	2	68866419	68866419	Human		name
401855862	CV2757563	single nucleotide variant	NM_014482.3(BMP10):c.464G>A (p.Arg155His)	not specified [RCV004340936]	uncertain significance	2	68866442	68866442	Human		name
401886277	CV2771142	single nucleotide variant	NM_014482.3(BMP10):c.380C>T (p.Pro127Leu)	not specified [RCV004346139]	uncertain significance	2	68866526	68866526	Human		name
405867079	CV2842594	single nucleotide variant	NM_014482.3(BMP10):c.370C>T (p.Arg124Ter)	EBV-positive nodal T- and NK-cell lymphoma [RCV004557951]	likely benign	2	68866536	68866536	Human		name
405749349	CV3291191	single nucleotide variant	NM_014482.3(BMP10):c.886G>A (p.Glu296Lys)	not specified [RCV004431861]	uncertain significance	2	68866020	68866020	Human		name
405854090	CV3395844	single nucleotide variant	NM_014482.3(BMP10):c.599C>G (p.Thr200Ser)	Bladder exstrophy-epispadias-cloacal extrophy complex [RCV004556175]\|not provided [RCV004810692]	benign\|likely benign	2	68866307	68866307	Human	1	name
407500167	CV3423941	single nucleotide variant	NM_014482.3(BMP10):c.649A>G (p.Thr217Ala)	not specified [RCV004607076]	uncertain significance	2	68866257	68866257	Human		name
407473965	CV3423943	single nucleotide variant	NM_014482.3(BMP10):c.563C>T (p.Ser188Phe)	not specified [RCV004600495]	uncertain significance	2	68866343	68866343	Human		name
596946946	CV3547004	single nucleotide variant	NM_014482.3(BMP10):c.625C>T (p.Arg209Cys)	not provided [RCV004810810]	likely benign	2	68866281	68866281	Human	1	name
596946946	CV3547004	single nucleotide variant	NM_014482.3(BMP10):c.625C>T (p.Arg209Cys)	not provided [RCV004810810]	likely benign	2	68866281	68866282	Human	1	name
597718261	CV3646705	single nucleotide variant	NM_014482.3(BMP10):c.848A>G (p.Asp283Gly)	not specified [RCV004887489]	uncertain significance	2	68866058	68866058	Human		name
597718270	CV3646706	single nucleotide variant	NM_014482.3(BMP10):c.411T>G (p.His137Gln)	not specified [RCV004887490]	uncertain significance	2	68866495	68866495	Human		name
597718281	CV3646707	single nucleotide variant	NM_014482.3(BMP10):c.866G>A (p.Ser289Asn)	not specified [RCV004887491]	uncertain significance	2	68866040	68866040	Human		name
15168440	CV719944	single nucleotide variant	NM_014482.3(BMP10):c.750C>A (p.Asn250Lys)	not provided [RCV000883064]	benign	2	68866156	68866156	Human	1	name
15168440	CV719944	single nucleotide variant	NM_014482.3(BMP10):c.750C>A (p.Asn250Lys)	not provided [RCV000883064]	benign	2	68866156	68866157	Human	1	name
156257881	CV2304826	single nucleotide variant	NM_014482.3(BMP10):c.1265G>C (p.Gly422Ala)	not specified [RCV004166965]	uncertain significance	2	68865641	68865641	Human		name

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