Sema6c Variant Search Result - Rat Genome Database

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15 records found for search term Sema6c

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15155455	CV777002	single nucleotide variant	NM_030913.6(SEMA6C):c.974+7A>C	not provided [RCV000946494]	benign	1	151136850	151136850	Human		name
15199523	CV729918	single nucleotide variant	NM_030913.6(SEMA6C):c.1434-6C>T	not provided [RCV000890658]	benign	1	151135315	151135315	Human		name
15169484	CV696085	single nucleotide variant	NM_030913.6(SEMA6C):c.91C>T (p.Leu31Phe)	not provided [RCV000949466]	benign	1	151142531	151142531	Human		name
156300630	CV2244951	single nucleotide variant	NM_030913.6(SEMA6C):c.274G>C (p.Gly92Arg)	not specified [RCV004104693]	uncertain significance	1	151139661	151139661	Human		name
155917961	CV2332911	single nucleotide variant	NM_030913.6(SEMA6C):c.790C>T (p.Arg264Cys)	not specified [RCV004192169]	uncertain significance	1	151137041	151137041	Human		name
156058733	CV2343645	single nucleotide variant	NM_030913.6(SEMA6C):c.575C>T (p.Ala192Val)	not specified [RCV004190673]	uncertain significance	1	151138078	151138078	Human		name
401932766	CV2809246	single nucleotide variant	NM_030913.6(SEMA6C):c.619C>T (p.Pro207Ser)	not provided [RCV003408862]	likely benign	1	151138034	151138034	Human		name
8624682	CV79796	single nucleotide variant	NM_001178061.1(SEMA6C):c.198C>T (p.Phe66=)	Malignant melanoma [RCV000059872]	not provided	1	151140011	151140011	Human		name
156134198	CV2235507	single nucleotide variant	NM_030913.6(SEMA6C):c.2356C>T (p.Pro786Ser)	not specified [RCV004109547]	uncertain significance	1	151132921	151132921	Human		name
156036584	CV2332458	single nucleotide variant	NM_030913.6(SEMA6C):c.2137C>T (p.Arg713Cys)	not specified [RCV004196185]	uncertain significance	1	151133140	151133140	Human		name
156256294	CV2359606	single nucleotide variant	NM_030913.6(SEMA6C):c.2126T>C (p.Val709Ala)	not specified [RCV004214904]	uncertain significance	1	151133151	151133151	Human		name
155929835	CV2360978	single nucleotide variant	NM_030913.6(SEMA6C):c.2432C>T (p.Pro811Leu)	not specified [RCV004216176]	uncertain significance	1	151132845	151132845	Human		name
155930129	CV2366565	single nucleotide variant	NM_030913.6(SEMA6C):c.1157G>A (p.Arg386Gln)	not specified [RCV004208537]	uncertain significance	1	151136113	151136113	Human		name
405694764	CV3226517	single nucleotide variant	NM_030913.6(SEMA6C):c.1922A>G (p.Glu641Gly)	not provided [RCV003992910]	likely benign	1	151133355	151133355	Human		name
15155450	CV696084	single nucleotide variant	NM_030913.6(SEMA6C):c.1628G>C (p.Arg543Thr)	not provided [RCV000946493]	benign	1	151134828	151134828	Human		name