Shisa4 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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17 records found for search term Shisa4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405731333	CV3314467	single nucleotide variant	NM_198149.3(SHISA4):c.10G>T (p.Ala4Ser)	not specified [RCV004451052]	uncertain significance	1	201889004	201889004	Human		name
405731340	CV3314468	single nucleotide variant	NM_198149.3(SHISA4):c.212C>A (p.Thr71Asn)	not specified [RCV004451053]	uncertain significance	1	201889583	201889583	Human		name
407493351	CV3480503	single nucleotide variant	NM_198149.3(SHISA4):c.247C>T (p.Pro83Ser)	not specified [RCV004667362]	uncertain significance	1	201890455	201890455	Human		name
597698738	CV3602595	single nucleotide variant	NM_198149.3(SHISA4):c.220C>G (p.Gln74Glu)	not specified [RCV004859669]	uncertain significance	1	201889591	201889591	Human		name
597698770	CV3602599	single nucleotide variant	NM_198149.3(SHISA4):c.100T>G (p.Tyr34Asp)	not specified [RCV004859673]	uncertain significance	1	201889471	201889471	Human		name
156153760	CV2242166	single nucleotide variant	NM_198149.3(SHISA4):c.442A>G (p.Lys148Glu)	not specified [RCV004109380]	uncertain significance	1	201891463	201891463	Human		name
155939333	CV2376685	single nucleotide variant	NM_198149.3(SHISA4):c.452C>G (p.Pro151Arg)	not specified [RCV004222881]	uncertain significance	1	201891473	201891473	Human		name
401742962	CV2697979	single nucleotide variant	NM_198149.3(SHISA4):c.386A>C (p.Glu129Ala)	not specified [RCV004302466]	uncertain significance	1	201891407	201891407	Human		name
401861032	CV2772679	single nucleotide variant	NM_198149.3(SHISA4):c.551C>T (p.Pro184Leu)	not specified [RCV004355416]	uncertain significance	1	201891803	201891803	Human		name
405731346	CV3314469	single nucleotide variant	NM_198149.3(SHISA4):c.347G>A (p.Arg116His)	not specified [RCV004451054]	uncertain significance	1	201890555	201890555	Human		name
405731354	CV3314470	single nucleotide variant	NM_198149.3(SHISA4):c.443A>C (p.Lys148Thr)	not specified [RCV004451055]	uncertain significance	1	201891464	201891464	Human		name
405731371	CV3314472	single nucleotide variant	NM_198149.3(SHISA4):c.455C>A (p.Ala152Glu)	not specified [RCV004451057]	uncertain significance	1	201891476	201891476	Human		name
407493347	CV3480502	single nucleotide variant	NM_198149.3(SHISA4):c.509C>T (p.Pro170Leu)	not specified [RCV004667361]	uncertain significance	1	201891530	201891530	Human		name
597698731	CV3602594	single nucleotide variant	NM_198149.3(SHISA4):c.323T>A (p.Leu108His)	not specified [RCV004859668]	uncertain significance	1	201890531	201890531	Human		name
597698747	CV3602596	single nucleotide variant	NM_198149.3(SHISA4):c.475A>G (p.Ile159Val)	not specified [RCV004859670]	uncertain significance	1	201891496	201891496	Human		name
597698754	CV3602597	single nucleotide variant	NM_198149.3(SHISA4):c.301G>A (p.Ala101Thr)	not specified [RCV004859671]	uncertain significance	1	201890509	201890509	Human		name
597698761	CV3602598	single nucleotide variant	NM_198149.3(SHISA4):c.503A>G (p.Gln168Arg)	not specified [RCV004859672]	uncertain significance	1	201891524	201891524	Human		name