Slc35c2 Variant Search Result - Rat Genome Database

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15 records found for search term Slc35c2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597765291	CV3603115	single nucleotide variant	NM_015945.12(SLC35C2):c.12G>T (p.Trp4Cys)	not specified [RCV004870335]	uncertain significance	20	46358495	46358495	Human		name
407509975	CV3484422	single nucleotide variant	NM_015945.12(SLC35C2):c.88G>A (p.Gly30Ser)	not specified [RCV004672590]	uncertain significance	20	46358419	46358419	Human		name
407510128	CV3484423	single nucleotide variant	NM_015945.12(SLC35C2):c.104A>G (p.Asn35Ser)	not specified [RCV004672591]	uncertain significance	20	46358403	46358403	Human		name
597765270	CV3603107	single nucleotide variant	NM_015945.12(SLC35C2):c.284C>T (p.Ala95Val)	not specified [RCV004870330]	uncertain significance	20	46356625	46356625	Human		name
597765287	CV3603114	single nucleotide variant	NM_015945.12(SLC35C2):c.123C>A (p.Ser41Arg)	not specified [RCV004870334]	uncertain significance	20	46357771	46357771	Human		name
597765295	CV3603116	single nucleotide variant	NM_015945.12(SLC35C2):c.229G>T (p.Val77Leu)	not specified [RCV004870336]	uncertain significance	20	46357665	46357665	Human		name
407509968	CV3484420	single nucleotide variant	NM_015945.12(SLC35C2):c.595G>A (p.Asp199Asn)	not specified [RCV004672588]	uncertain significance	20	46354948	46354948	Human		name
407509972	CV3484421	single nucleotide variant	NM_015945.12(SLC35C2):c.698T>G (p.Phe233Cys)	not specified [RCV004672589]	uncertain significance	20	46352190	46352190	Human		name
597702152	CV3603109	single nucleotide variant	NM_015945.12(SLC35C2):c.445G>C (p.Gly149Arg)	not specified [RCV004860064]	uncertain significance	20	46355205	46355205	Human		name
597765278	CV3603110	single nucleotide variant	NM_015945.12(SLC35C2):c.413C>T (p.Ala138Val)	not specified [RCV004870332]	uncertain significance	20	46355237	46355237	Human		name
597702163	CV3603111	single nucleotide variant	NM_015945.12(SLC35C2):c.937C>T (p.His313Tyr)	not specified [RCV004860065]	uncertain significance	20	46350791	46350791	Human		name
597765282	CV3603112	single nucleotide variant	NM_015945.12(SLC35C2):c.940G>A (p.Val314Ile)	not specified [RCV004870333]	uncertain significance	20	46350788	46350788	Human		name
597702185	CV3603117	single nucleotide variant	NM_015945.12(SLC35C2):c.877G>A (p.Asp293Asn)	not specified [RCV004860067]	uncertain significance	20	46350851	46350851	Human		name
597702194	CV3603118	single nucleotide variant	NM_015945.12(SLC35C2):c.686A>T (p.Lys229Ile)	not specified [RCV004860068]	uncertain significance	20	46352202	46352202	Human		name
597765274	CV3603108	single nucleotide variant	NM_015945.12(SLC35C2):c.1043G>A (p.Arg348Gln)	not specified [RCV004870331]	likely benign	20	46350449	46350449	Human		name