Ubb Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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14 records found for search term Ubb

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15123775	CV771260	single nucleotide variant	NM_018955.4(UBB):c.27C>T (p.Thr9=)	not provided [RCV000940913]	likely benign	17	16381934	16381934	Human		name
15194062	CV727003	single nucleotide variant	NM_018955.4(UBB):c.57C>T (p.Pro19=)	not provided [RCV000889115]	benign	17	16381964	16381964	Human		name
15097638	CV727004	single nucleotide variant	NM_018955.4(UBB):c.99G>A (p.Lys33=)	not provided [RCV000891548]	likely benign	17	16382006	16382006	Human		name
15126521	CV755623	single nucleotide variant	NM_018955.4(UBB):c.297C>T (p.Ile99=)	not provided [RCV000919339]	likely benign	17	16382204	16382204	Human		name
8627924	CV83068	single nucleotide variant	NM_018955.3(UBB):c.150G>A (p.Leu50=)	Malignant melanoma [RCV000063148]	not provided	17	16382057	16382057	Human		name
596920369	CV3534552	single nucleotide variant	NM_018955.4(UBB):c.91C>T (p.Gln31Ter)	not specified [RCV004782113]	uncertain significance	17	16381998	16381998	Human		name
15160606	CV727005	single nucleotide variant	NM_018955.4(UBB):c.618C>T (p.Arg206=)	not provided [RCV000881413]	likely benign	17	16382525	16382525	Human		name
15107287	CV727006	single nucleotide variant	NM_018955.4(UBB):c.645A>G (p.Lys215=)	not provided [RCV000893446]	likely benign	17	16382552	16382552	Human		name
15160060	CV740585	single nucleotide variant	NM_018955.4(UBB):c.567C>T (p.Pro189=)	not provided [RCV000903067]	likely benign	17	16382474	16382474	Human		name
15159485	CV740586	single nucleotide variant	NM_018955.4(UBB):c.585C>T (p.Leu195=)	not provided [RCV000902948]	likely benign	17	16382492	16382492	Human		name
598264942	CV3932683	single nucleotide variant	NM_018955.4(UBB):c.230T>C (p.Met77Thr)	not specified [RCV005301633]	uncertain significance	17	16382137	16382137	Human		name
8627923	CV83067	single nucleotide variant	NM_018955.3(UBB):c.143A>T (p.Lys48Met)	Malignant melanoma [RCV000063147]	not provided	17	16382050	16382050	Human		name
8627925	CV83069	single nucleotide variant	NM_018955.3(UBB):c.160C>T (p.Arg54Cys)	Malignant melanoma [RCV000063149]	not provided	17	16382067	16382067	Human		name
156062247	CV2320975	single nucleotide variant	NM_018955.4(UBB):c.539C>T (p.Ala180Val)	not specified [RCV004172775]	uncertain significance	17	16382446	16382446	Human		name