Ly6g6f Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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29 records found for search term Ly6g6f

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597644810	CV3699905	single nucleotide variant	NM_001003693.3(LY6G6F):c.64G>A (p.Ala22Thr)	not specified [RCV004942259]	uncertain significance	6	31707469	31707469	Human		name
155964558	CV2261652	single nucleotide variant	NM_001003693.3(LY6G6F):c.112C>T (p.Pro38Ser)	not specified [RCV004125974]	uncertain significance	6	31707517	31707517	Human		name
329350003	CV2462114	single nucleotide variant	NM_001003693.3(LY6G6F):c.226A>C (p.Lys76Gln)	not specified [RCV004266141]	uncertain significance	6	31707631	31707631	Human		name
401744812	CV2685233	single nucleotide variant	NM_001003693.3(LY6G6F):c.275G>C (p.Trp92Ser)	not specified [RCV004289784]	uncertain significance	6	31707680	31707680	Human		name
401858307	CV2757881	single nucleotide variant	NM_001003693.3(LY6G6F):c.133G>A (p.Glu45Lys)	not specified [RCV004337022]	uncertain significance	6	31707538	31707538	Human		name
405815972	CV3280903	single nucleotide variant	NM_001003693.3(LY6G6F):c.118A>G (p.Thr40Ala)	not specified [RCV004410957]	uncertain significance	6	31707523	31707523	Human		name
597644788	CV3699902	single nucleotide variant	NM_001003693.3(LY6G6F):c.292G>C (p.Glu98Gln)	not specified [RCV004942256]	uncertain significance	6	31707697	31707697	Human		name
597644796	CV3699903	single nucleotide variant	NM_001003693.3(LY6G6F):c.229C>T (p.Pro77Ser)	not specified [RCV004942257]	uncertain significance	6	31707634	31707634	Human		name
598163690	CV3981370	single nucleotide variant	NM_001003693.3(LY6G6F):c.199G>C (p.Val67Leu)	not specified [RCV005368870]	uncertain significance	6	31707604	31707604	Human		name
598182490	CV3981371	single nucleotide variant	NM_001003693.3(LY6G6F):c.272T>C (p.Leu91Ser)	not specified [RCV005372753]	uncertain significance	6	31707677	31707677	Human		name
15117132	CV717901	single nucleotide variant	NM_001003693.3(LY6G6F):c.101C>A (p.Pro34Gln)	not provided [RCV000962151]	benign	6	31707506	31707506	Human		name
156041722	CV2219595	single nucleotide variant	NM_001003693.3(LY6G6F):c.850A>T (p.Ile284Phe)	not specified [RCV004095323]	uncertain significance	6	31710399	31710399	Human		name
156037287	CV2243763	single nucleotide variant	NM_001003693.3(LY6G6F):c.515C>T (p.Ser172Phe)	not specified [RCV004114456]	uncertain significance	6	31708003	31708003	Human		name
156301689	CV2258534	single nucleotide variant	NM_001003693.3(LY6G6F):c.505C>T (p.Arg169Cys)	not specified [RCV004116020]	uncertain significance	6	31707993	31707993	Human		name
156066505	CV2340905	single nucleotide variant	NM_001003693.3(LY6G6F):c.862C>T (p.Arg288Cys)	not specified [RCV004181402]	uncertain significance	6	31710411	31710411	Human		name
329349714	CV2424458	single nucleotide variant	NM_001003693.3(LY6G6F):c.497T>G (p.Val166Gly)	not specified [RCV004252349]	uncertain significance	6	31707985	31707985	Human		name
329349545	CV2449438	single nucleotide variant	NM_001003693.3(LY6G6F):c.313T>G (p.Trp105Gly)	not specified [RCV004266597]	uncertain significance	6	31707718	31707718	Human		name
401746062	CV2684406	single nucleotide variant	NM_001003693.3(LY6G6F):c.398C>T (p.Ala133Val)	not specified [RCV004291485]	uncertain significance	6	31707886	31707886	Human		name
401768684	CV2686338	single nucleotide variant	NM_001003693.3(LY6G6F):c.848A>G (p.Asn283Ser)	not specified [RCV004297414]	uncertain significance	6	31710397	31710397	Human		name
401857679	CV2759970	single nucleotide variant	NM_001003693.3(LY6G6F):c.416C>A (p.Ser139Tyr)	not specified [RCV004345388]	uncertain significance	6	31707904	31707904	Human		name
405815973	CV3280904	single nucleotide variant	NM_001003693.3(LY6G6F):c.709C>G (p.Leu237Val)	not specified [RCV004410958]	uncertain significance	6	31710088	31710088	Human		name
405815974	CV3280905	single nucleotide variant	NM_001003693.3(LY6G6F):c.787G>T (p.Gly263Trp)	not specified [RCV004410959]	uncertain significance	6	31710166	31710166	Human		name
405815975	CV3280906	single nucleotide variant	NM_001003693.3(LY6G6F):c.809C>T (p.Ser270Leu)	not specified [RCV004410960]	uncertain significance	6	31710358	31710358	Human		name
597644803	CV3699904	single nucleotide variant	NM_001003693.3(LY6G6F):c.727A>G (p.Met243Val)	not specified [RCV004942258]	likely benign	6	31710106	31710106	Human		name
597644817	CV3699906	single nucleotide variant	NM_001003693.3(LY6G6F):c.640C>A (p.Leu214Met)	not specified [RCV004942260]	uncertain significance	6	31708128	31708128	Human		name
597644824	CV3699908	single nucleotide variant	NM_001003693.3(LY6G6F):c.784C>T (p.Arg262Cys)	not specified [RCV004942261]	uncertain significance	6	31710163	31710163	Human		name
598182479	CV3981367	single nucleotide variant	NM_001003693.3(LY6G6F):c.602G>T (p.Arg201Leu)	not specified [RCV005372751]	uncertain significance	6	31708090	31708090	Human		name
598182486	CV3981368	single nucleotide variant	NM_001003693.3(LY6G6F):c.442G>A (p.Val148Met)	not specified [RCV005372752]	uncertain significance	6	31707930	31707930	Human		name
598163684	CV3981369	single nucleotide variant	NM_001003693.3(LY6G6F):c.698T>C (p.Met233Thr)	not specified [RCV005368869]	uncertain significance	6	31710077	31710077	Human		name

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