Gapt 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 Gapt

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15145155	CV709957	single nucleotide variant	NM_001304431.2(GAPT):c.240C>T (p.His80=)	not provided [RCV000966947]	benign	5	58494776	58494776	Human		name
405750796	CV3251170	single nucleotide variant	NM_001304431.2(GAPT):c.29C>T (p.Ala10Val)	not specified [RCV004392707]	likely benign	5	58494565	58494565	Human		name
597780142	CV3680851	single nucleotide variant	NM_001304431.2(GAPT):c.74G>A (p.Cys25Tyr)	not specified [RCV004930554]	uncertain significance	5	58494610	58494610	Human		name
155915239	CV2274060	single nucleotide variant	NM_001304431.2(GAPT):c.241A>G (p.Lys81Glu)	not specified [RCV004134712]	uncertain significance	5	58494777	58494777	Human		name
155907203	CV2354382	single nucleotide variant	NM_001304431.2(GAPT):c.202G>A (p.Gly68Ser)	not specified [RCV004200336]	likely benign	5	58494738	58494738	Human		name
329362318	CV2463811	single nucleotide variant	NM_001304431.2(GAPT):c.173C>A (p.Thr58Asn)	not specified [RCV004279900]	uncertain significance	5	58494709	58494709	Human		name
329374909	CV2470810	single nucleotide variant	NM_001304431.2(GAPT):c.212A>G (p.His71Arg)	not specified [RCV004276024]	uncertain significance	5	58494748	58494748	Human		name
401750562	CV2689454	single nucleotide variant	NM_001304431.2(GAPT):c.109G>T (p.Val37Phe)	not specified [RCV004306256]	uncertain significance	5	58494645	58494645	Human		name
401768402	CV2716559	single nucleotide variant	NM_001304431.2(GAPT):c.250G>C (p.Val84Leu)	not specified [RCV004327635]	uncertain significance	5	58494786	58494786	Human		name
405750788	CV3251169	single nucleotide variant	NM_001304431.2(GAPT):c.206T>C (p.Leu69Ser)	not specified [RCV004392706]	likely benign	5	58494742	58494742	Human		name
597754352	CV3680852	single nucleotide variant	NM_001304431.2(GAPT):c.136T>G (p.Phe46Val)	not specified [RCV004924353]	uncertain significance	5	58494672	58494672	Human		name
598158894	CV3974023	single nucleotide variant	NM_001304431.2(GAPT):c.213T>A (p.His71Gln)	not specified [RCV005328155]	uncertain significance	5	58494749	58494749	Human		name
15127093	CV709958	single nucleotide variant	NM_001304431.2(GAPT):c.247G>A (p.Ala83Thr)	not provided [RCV000963844]	benign	5	58494783	58494783	Human		name
156113856	CV2397099	single nucleotide variant	NM_001304431.2(GAPT):c.449T>C (p.Ile150Thr)	not specified [RCV004236606]	uncertain significance	5	58494985	58494985	Human		name
401881751	CV2784808	single nucleotide variant	NM_001304431.2(GAPT):c.332T>C (p.Leu111Pro)	not specified [RCV004352598]	uncertain significance	5	58494868	58494868	Human		name
405750803	CV3251171	single nucleotide variant	NM_001304431.2(GAPT):c.401A>G (p.Tyr134Cys)	not specified [RCV004392708]	uncertain significance	5	58494937	58494937	Human		name
407462159	CV3436378	single nucleotide variant	NM_001304431.2(GAPT):c.395A>G (p.Asp132Gly)	not specified [RCV004634460]	uncertain significance	5	58494931	58494931	Human		name