Ankrd46 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 Ankrd46

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8632743	CV87958	single nucleotide variant	NM_198401.3(ANKRD46):c.121C>T (p.Arg41Cys)	Malignant melanoma [RCV000068050]	not provided	8	100529713	100529713	Human		name
156363561	CV2265762	single nucleotide variant	NM_001270377.2(ANKRD46):c.40G>A (p.Val14Met)	not specified [RCV004124470]	uncertain significance	8	100529794	100529794	Human		name
405683754	CV3282223	single nucleotide variant	NM_001270377.2(ANKRD46):c.34A>G (p.Thr12Ala)	not specified [RCV004422202]	uncertain significance	8	100529800	100529800	Human		name
597638556	CV3554483	single nucleotide variant	NM_001270377.2(ANKRD46):c.61A>G (p.Ile21Val)	not specified [RCV004824950]	uncertain significance	8	100529773	100529773	Human		name
156065008	CV2287248	single nucleotide variant	NM_001270377.2(ANKRD46):c.265G>T (p.Asp89Tyr)	not specified [RCV004146892]	uncertain significance	8	100529569	100529569	Human		name
405683530	CV3282211	single nucleotide variant	NM_001270377.2(ANKRD46):c.137G>A (p.Arg46Lys)	not specified [RCV004422190]	uncertain significance	8	100529697	100529697	Human		name
405683784	CV3282215	single nucleotide variant	NM_001270377.2(ANKRD46):c.176A>G (p.Asp59Gly)	not specified [RCV004422194]	uncertain significance	8	100529658	100529658	Human		name
597638561	CV3554484	single nucleotide variant	NM_001270377.2(ANKRD46):c.208G>A (p.Asp70Asn)	not specified [RCV004824951]	uncertain significance	8	100529626	100529626	Human		name
156056131	CV2320588	single nucleotide variant	NM_001270377.2(ANKRD46):c.497A>G (p.Asn166Ser)	not specified [RCV004172209]	uncertain significance	8	100522745	100522745	Human		name
329374185	CV2463421	single nucleotide variant	NM_001270377.2(ANKRD46):c.369T>G (p.Asp123Glu)	not specified [RCV004277256]	uncertain significance	8	100527946	100527946	Human		name
405683714	CV3282234	single nucleotide variant	NM_001270377.2(ANKRD46):c.445A>G (p.Thr149Ala)	not specified [RCV004422213]	uncertain significance	8	100527870	100527870	Human		name
405683574	CV3282238	single nucleotide variant	NM_001270377.2(ANKRD46):c.533G>C (p.Ser178Thr)	not specified [RCV004422217]	uncertain significance	8	100522709	100522709	Human		name
405683555	CV3282242	single nucleotide variant	NM_001270377.2(ANKRD46):c.634T>C (p.Tyr212His)	not specified [RCV004422221]	uncertain significance	8	100522608	100522608	Human		name
405683563	CV3282244	single nucleotide variant	NM_001270377.2(ANKRD46):c.673G>A (p.Glu225Lys)	not specified [RCV004422223]	uncertain significance	8	100522569	100522569	Human		name
407515366	CV3450704	single nucleotide variant	NM_001270377.2(ANKRD46):c.658G>A (p.Val220Met)	not specified [RCV004649869]	uncertain significance	8	100522584	100522584	Human		name
597638567	CV3554485	single nucleotide variant	NM_001270377.2(ANKRD46):c.349C>T (p.Arg117Cys)	not specified [RCV004824952]	uncertain significance	8	100527966	100527966	Human		name
598187805	CV3989381	single nucleotide variant	NM_001270377.2(ANKRD46):c.367G>A (p.Asp123Asn)	not specified [RCV005373620]	uncertain significance	8	100527948	100527948	Human		name