Cabp7 Variant Search Result - Rat Genome Database

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19 records found for search term Cabp7

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155977488	CV2266416	single nucleotide variant	NM_182527.3(CABP7):c.148A>G (p.Asn50Asp)	not specified [RCV004131007]	uncertain significance	22	29727700	29727700	Human		name
405751113	CV3291617	single nucleotide variant	NM_182527.3(CABP7):c.211G>A (p.Glu71Lys)	not specified [RCV004432118]	uncertain significance	22	29727763	29727763	Human		name
405751118	CV3291618	single nucleotide variant	NM_182527.3(CABP7):c.251A>G (p.Asp84Gly)	not specified [RCV004432119]	uncertain significance	22	29727803	29727803	Human		name
407496546	CV3428057	single nucleotide variant	NM_182527.3(CABP7):c.249G>A (p.Met83Ile)	not specified [RCV004606121]	uncertain significance	22	29727801	29727801	Human		name
407496554	CV3428060	single nucleotide variant	NM_182527.3(CABP7):c.111G>T (p.Glu37Asp)	not specified [RCV004606123]	uncertain significance	22	29727663	29727663	Human		name
597762651	CV3640769	single nucleotide variant	NM_182527.3(CABP7):c.238C>T (p.Arg80Trp)	not specified [RCV004895194]	uncertain significance	22	29727790	29727790	Human		name
597762662	CV3640772	single nucleotide variant	NM_182527.3(CABP7):c.254G>A (p.Gly85Asp)	not specified [RCV004895196]	uncertain significance	22	29728630	29728630	Human		name
156327687	CV2219903	single nucleotide variant	NM_182527.3(CABP7):c.386C>T (p.Thr129Met)	not specified [RCV004095532]	uncertain significance	22	29729074	29729074	Human		name
156075814	CV2248278	single nucleotide variant	NM_182527.3(CABP7):c.641T>A (p.Met214Lys)	not specified [RCV004119444]	uncertain significance	22	29729562	29729562	Human		name
156232220	CV2273663	single nucleotide variant	NM_182527.3(CABP7):c.531C>A (p.Asn177Lys)	not specified [RCV004132327]	uncertain significance	22	29729452	29729452	Human		name
156119936	CV2354127	single nucleotide variant	NM_182527.3(CABP7):c.551G>A (p.Cys184Tyr)	not specified [RCV004206564]	uncertain significance	22	29729472	29729472	Human		name
156094836	CV2377828	single nucleotide variant	NM_182527.3(CABP7):c.370G>A (p.Asp124Asn)	not specified [RCV004230404]	uncertain significance	22	29729058	29729058	Human		name
329367517	CV2456884	single nucleotide variant	NM_182527.3(CABP7):c.320T>A (p.Ile107Asn)	not specified [RCV004270842]	uncertain significance	22	29728696	29728696	Human		name
329389007	CV2469693	single nucleotide variant	NM_182527.3(CABP7):c.383T>C (p.Leu128Pro)	not specified [RCV004283106]	uncertain significance	22	29729071	29729071	Human		name
329393939	CV2472220	single nucleotide variant	NM_182527.3(CABP7):c.496G>A (p.Glu166Lys)	not specified [RCV004283336]	uncertain significance	22	29729184	29729184	Human		name
401751897	CV2672613	single nucleotide variant	NM_182527.3(CABP7):c.403C>T (p.Arg135Trp)	not specified [RCV004287642]	uncertain significance	22	29729091	29729091	Human		name
597750400	CV3640770	single nucleotide variant	NM_182527.3(CABP7):c.467C>T (p.Thr156Met)	not specified [RCV004892576]	uncertain significance	22	29729155	29729155	Human		name
597762656	CV3640771	single nucleotide variant	NM_182527.3(CABP7):c.353C>T (p.Thr118Ile)	not specified [RCV004895195]	uncertain significance	22	29728729	29728729	Human		name
598212040	CV3946434	single nucleotide variant	NM_182527.3(CABP7):c.614C>T (p.Ala205Val)	not specified [RCV005316105]	uncertain significance	22	29729535	29729535	Human		name

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