Anxa8 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 Anxa8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401938260	CV2813126	single nucleotide variant	NM_001098845.3(ANXA8L1):c.951C>T (p.Asn317=)	not provided [RCV003417348]	benign	10	46390897	46390897	Human		name
598263961	CV3983053	single nucleotide variant	NM_001098845.3(ANXA8L1):c.94A>C (p.Lys32Gln)	not specified [RCV005387628]	uncertain significance	10	46379957	46379957	Human		name
401784219	CV2721161	single nucleotide variant	NM_001098845.3(ANXA8L1):c.130A>G (p.Ile44Val)	not specified [RCV004330149]	uncertain significance	10	46381163	46381163	Human		name
405696779	CV3278855	single nucleotide variant	NM_001098845.3(ANXA8L1):c.178G>A (p.Ala60Thr)	not specified [RCV004424676]	uncertain significance	10	46381211	46381211	Human		name
405696784	CV3278856	single nucleotide variant	NM_001098845.3(ANXA8L1):c.280C>T (p.Pro94Ser)	not specified [RCV004424677]	uncertain significance	10	46382651	46382651	Human		name
156188990	CV2258460	single nucleotide variant	NM_001098845.3(ANXA8L1):c.944A>T (p.Tyr315Phe)	not specified [RCV004115652]	uncertain significance	10	46390890	46390890	Human		name
329388316	CV2468890	single nucleotide variant	NM_001098845.3(ANXA8L1):c.362C>T (p.Ala121Val)	not specified [RCV004280193]	uncertain significance	10	46383496	46383496	Human		name
401868107	CV2767150	single nucleotide variant	NM_001098845.3(ANXA8L1):c.952G>A (p.Ala318Thr)	not specified [RCV004347547]	uncertain significance	10	46390898	46390898	Human		name
401899017	CV2785948	single nucleotide variant	NM_001098845.3(ANXA8L1):c.375G>T (p.Lys125Asn)	not specified [RCV004359793]	uncertain significance	10	46383509	46383509	Human		name
405696797	CV3278858	single nucleotide variant	NM_001098845.3(ANXA8L1):c.547G>A (p.Ala183Thr)	not specified [RCV004424679]	uncertain significance	10	46384828	46384828	Human		name
405696805	CV3278859	single nucleotide variant	NM_001098845.3(ANXA8L1):c.620C>T (p.Thr207Met)	not specified [RCV004424680]	uncertain significance	10	46385447	46385447	Human		name
597652751	CV3555418	single nucleotide variant	NM_001098845.3(ANXA8L1):c.524A>G (p.Asp175Gly)	not specified [RCV004833861]	uncertain significance	10	46384805	46384805	Human		name
598229956	CV3983044	single nucleotide variant	NM_001098845.3(ANXA8L1):c.346A>G (p.Ile116Val)	not specified [RCV005381110]	uncertain significance	10	46383480	46383480	Human		name
598230059	CV3983064	single nucleotide variant	NM_001098845.3(ANXA8L1):c.513C>A (p.Ser171Arg)	not specified [RCV005381126]	uncertain significance	10	46384794	46384794	Human		name