Hs3st3b1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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41 records found for search term Hs3st3b1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405798954	CV3274053	single nucleotide variant	NM_006041.3(HS3ST3B1):c.5G>T (p.Gly2Val)	not specified [RCV004402378]	uncertain significance	17	14301523	14301523	Human		name
15190532	CV703969	single nucleotide variant	NM_006041.3(HS3ST3B1):c.33C>T (p.Cys11=)	not provided [RCV000954504]	benign	17	14301551	14301551	Human		name
156066417	CV2349027	single nucleotide variant	NM_006041.3(HS3ST3B1):c.22G>C (p.Gly8Arg)	not specified [RCV004203452]	uncertain significance	17	14301540	14301540	Human		name
405798945	CV3274050	single nucleotide variant	NM_006041.3(HS3ST3B1):c.17G>C (p.Ser6Thr)	not specified [RCV004402375]	uncertain significance	17	14301535	14301535	Human		name
407458086	CV3433955	single nucleotide variant	NM_006041.3(HS3ST3B1):c.34C>T (p.Leu12Phe)	not specified [RCV004633138]	uncertain significance	17	14301552	14301552	Human		name
407510845	CV3433958	single nucleotide variant	NM_006041.3(HS3ST3B1):c.41T>C (p.Val14Ala)	not specified [RCV004626266]	uncertain significance	17	14301559	14301559	Human		name
597773508	CV3689566	single nucleotide variant	NM_006041.3(HS3ST3B1):c.47G>T (p.Gly16Val)	not specified [RCV004928917]	uncertain significance	17	14301565	14301565	Human		name
598193015	CV3972024	single nucleotide variant	NM_006041.3(HS3ST3B1):c.80C>T (p.Pro27Leu)	not specified [RCV005354570]	uncertain significance	17	14301598	14301598	Human		name
15106315	CV726988	single nucleotide variant	NM_006041.3(HS3ST3B1):c.53T>A (p.Leu18His)	not provided [RCV000893256]	benign	17	14301571	14301571	Human		name
15154933	CV726989	single nucleotide variant	NM_006041.3(HS3ST3B1):c.333G>A (p.Pro111=)	not provided [RCV000880315]	benign	17	14301851	14301851	Human		name
156281351	CV2220512	single nucleotide variant	NM_006041.3(HS3ST3B1):c.169G>T (p.Ala57Ser)	not specified [RCV004097735]	uncertain significance	17	14301687	14301687	Human		name
155943657	CV2294798	single nucleotide variant	NM_006041.3(HS3ST3B1):c.235A>T (p.Thr79Ser)	not specified [RCV004162310]	uncertain significance	17	14301753	14301753	Human		name
156053263	CV2329080	single nucleotide variant	NM_006041.3(HS3ST3B1):c.100G>C (p.Ala34Pro)	not specified [RCV004180350]	uncertain significance	17	14301618	14301618	Human		name
156104371	CV2400285	single nucleotide variant	NM_006041.3(HS3ST3B1):c.272G>T (p.Arg91Leu)	not specified [RCV004244345]	uncertain significance	17	14301790	14301790	Human		name
405798942	CV3274049	single nucleotide variant	NM_006041.3(HS3ST3B1):c.115A>G (p.Met39Val)	not specified [RCV004402374]	uncertain significance	17	14301633	14301633	Human		name
405798949	CV3274051	single nucleotide variant	NM_006041.3(HS3ST3B1):c.260G>C (p.Arg87Thr)	not specified [RCV004402376]	uncertain significance	17	14301778	14301778	Human		name
407458082	CV3433954	single nucleotide variant	NM_006041.3(HS3ST3B1):c.200G>T (p.Gly67Val)	not specified [RCV004633137]	uncertain significance	17	14301718	14301718	Human		name
597773514	CV3689568	single nucleotide variant	NM_006041.3(HS3ST3B1):c.142C>G (p.Leu48Val)	not specified [RCV004928918]	uncertain significance	17	14301660	14301660	Human		name
597773525	CV3689570	single nucleotide variant	NM_006041.3(HS3ST3B1):c.193G>C (p.Gly65Arg)	not specified [RCV004928920]	uncertain significance	17	14301711	14301711	Human		name
156120356	CV2233661	single nucleotide variant	NM_006041.3(HS3ST3B1):c.739G>A (p.Asp247Asn)	not specified [RCV004100115]	uncertain significance	17	14345212	14345212	Human		name
155924166	CV2280481	single nucleotide variant	NM_006041.3(HS3ST3B1):c.398G>A (p.Gly133Glu)	not specified [RCV004142687]	uncertain significance	17	14301916	14301916	Human		name
156186339	CV2295013	single nucleotide variant	NM_006041.3(HS3ST3B1):c.733C>G (p.Arg245Gly)	not specified [RCV004156146]	uncertain significance	17	14345206	14345206	Human		name
155954402	CV2303392	single nucleotide variant	NM_006041.3(HS3ST3B1):c.421A>G (p.Ile141Val)	not specified [RCV004159121]	uncertain significance	17	14301939	14301939	Human		name
155999671	CV2373445	single nucleotide variant	NM_006041.3(HS3ST3B1):c.623G>C (p.Arg208Pro)	not specified [RCV004220143]	uncertain significance	17	14345096	14345096	Human		name
155937146	CV2376322	single nucleotide variant	NM_006041.3(HS3ST3B1):c.328A>T (p.Ser110Cys)	not specified [RCV004222582]	uncertain significance	17	14301846	14301846	Human		name
155992938	CV2381657	single nucleotide variant	NM_006041.3(HS3ST3B1):c.958A>T (p.Ile320Phe)	not specified [RCV004232127]	uncertain significance	17	14345431	14345431	Human		name
329363494	CV2442221	single nucleotide variant	NM_006041.3(HS3ST3B1):c.332C>G (p.Pro111Arg)	not specified [RCV004264713]	uncertain significance	17	14301850	14301850	Human		name
329397401	CV2466116	single nucleotide variant	NM_006041.3(HS3ST3B1):c.519C>G (p.Phe173Leu)	not specified [RCV004279776]	uncertain significance	17	14302037	14302037	Human		name
329392941	CV2469087	single nucleotide variant	NM_006041.3(HS3ST3B1):c.987C>A (p.Asn329Lys)	not specified [RCV004274324]	uncertain significance	17	14345460	14345460	Human		name
401865370	CV2754240	single nucleotide variant	NM_006041.3(HS3ST3B1):c.311T>C (p.Met104Thr)	not specified [RCV004334426]	uncertain significance	17	14301829	14301829	Human		name
401858735	CV2770621	single nucleotide variant	NM_006041.3(HS3ST3B1):c.607A>G (p.Ser203Gly)	not specified [RCV004349675]	uncertain significance	17	14345080	14345080	Human		name
401881470	CV2784609	single nucleotide variant	NM_006041.3(HS3ST3B1):c.902T>C (p.Ile301Thr)	not specified [RCV004352445]	uncertain significance	17	14345375	14345375	Human		name
405798952	CV3274052	single nucleotide variant	NM_006041.3(HS3ST3B1):c.467T>G (p.Phe156Cys)	not specified [RCV004402377]	uncertain significance	17	14301985	14301985	Human		name
407458090	CV3433956	single nucleotide variant	NM_006041.3(HS3ST3B1):c.888C>A (p.Ser296Arg)	not specified [RCV004633139]	uncertain significance	17	14345361	14345361	Human		name
407510842	CV3433957	single nucleotide variant	NM_006041.3(HS3ST3B1):c.302G>A (p.Gly101Asp)	not specified [RCV004626265]	uncertain significance	17	14301820	14301820	Human		name
597773502	CV3689565	single nucleotide variant	NM_006041.3(HS3ST3B1):c.762G>C (p.Leu254Phe)	not specified [RCV004928916]	uncertain significance	17	14345235	14345235	Human		name
597773520	CV3689569	single nucleotide variant	NM_006041.3(HS3ST3B1):c.921G>C (p.Glu307Asp)	not specified [RCV004928919]	uncertain significance	17	14345394	14345394	Human		name
597773530	CV3689571	single nucleotide variant	NM_006041.3(HS3ST3B1):c.346C>T (p.Pro116Ser)	not specified [RCV004928921]	uncertain significance	17	14301864	14301864	Human		name
598193009	CV3972022	single nucleotide variant	NM_006041.3(HS3ST3B1):c.346C>A (p.Pro116Thr)	not specified [RCV005354569]	uncertain significance	17	14301864	14301864	Human		name
405798939	CV3274048	single nucleotide variant	NM_006041.3(HS3ST3B1):c.1105C>A (p.Arg369Ser)	not specified [RCV004402373]	uncertain significance	17	14345578	14345578	Human		name
598205462	CV3972023	single nucleotide variant	NM_006041.3(HS3ST3B1):c.1157A>T (p.Asp386Val)	not specified [RCV005337614]	uncertain significance	17	14345630	14345630	Human		name

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