Tmem88 Variant Search Result - Rat Genome Database

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37 records found for search term Tmem88

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407526992	CV3482855	single nucleotide variant	NM_203411.2(TMEM88):c.7G>A (p.Asp3Asn)	not specified [RCV004679843]	uncertain significance	17	7855081	7855081	Human		name
401882166	CV2793390	single nucleotide variant	NM_203411.2(TMEM88):c.26G>A (p.Arg9Gln)	not specified [RCV004362491]	uncertain significance	17	7855100	7855100	Human		name
405772462	CV3343302	single nucleotide variant	NM_203411.2(TMEM88):c.14C>G (p.Pro5Arg)	not specified [RCV004470529]	uncertain significance	17	7855088	7855088	Human		name
156253145	CV2212514	single nucleotide variant	NM_203411.2(TMEM88):c.73T>G (p.Trp25Gly)	not specified [RCV004091398]	uncertain significance	17	7855147	7855147	Human		name
156293699	CV2321340	single nucleotide variant	NM_203411.2(TMEM88):c.34C>T (p.Pro12Ser)	not specified [RCV004177344]	uncertain significance	17	7855108	7855108	Human		name
401753484	CV2722485	single nucleotide variant	NM_203411.2(TMEM88):c.91G>C (p.Val31Leu)	not specified [RCV004322873]	uncertain significance	17	7855165	7855165	Human		name
405772478	CV3343305	single nucleotide variant	NM_203411.2(TMEM88):c.91G>T (p.Val31Leu)	not specified [RCV004470532]	uncertain significance	17	7855165	7855165	Human		name
598252790	CV3914086	single nucleotide variant	NM_203411.2(TMEM88):c.32T>A (p.Val11Asp)	not specified [RCV005278142]	uncertain significance	17	7855106	7855106	Human		name
155918200	CV2195793	single nucleotide variant	NM_203411.2(TMEM88):c.250C>G (p.Arg84Gly)	not specified [RCV004076143]	uncertain significance	17	7855484	7855484	Human		name
156243508	CV2347081	single nucleotide variant	NM_203411.2(TMEM88):c.217C>G (p.Arg73Gly)	not specified [RCV004204564]	uncertain significance	17	7855451	7855451	Human		name
407526995	CV3482856	single nucleotide variant	NM_203411.2(TMEM88):c.251G>A (p.Arg84Gln)	not specified [RCV004679844]	uncertain significance	17	7855485	7855485	Human		name
597800744	CV3610725	single nucleotide variant	NM_203411.2(TMEM88):c.217C>T (p.Arg73Cys)	not specified [RCV004880372]	uncertain significance	17	7855451	7855451	Human		name
597800746	CV3610726	single nucleotide variant	NM_203411.2(TMEM88):c.125A>G (p.Asn42Ser)	not specified [RCV004880373]	uncertain significance	17	7855199	7855199	Human		name
598227751	CV3914083	single nucleotide variant	NM_203411.2(TMEM88):c.242C>T (p.Ala81Val)	not specified [RCV005294633]	uncertain significance	17	7855476	7855476	Human		name
598227758	CV3914084	single nucleotide variant	NM_203411.2(TMEM88):c.213C>A (p.Phe71Leu)	not specified [RCV005294634]	uncertain significance	17	7855447	7855447	Human		name
598227767	CV3914085	single nucleotide variant	NM_203411.2(TMEM88):c.101A>G (p.Gln34Arg)	not specified [RCV005294635]	uncertain significance	17	7855175	7855175	Human		name
156065480	CV2196937	single nucleotide variant	NM_203411.2(TMEM88):c.454C>G (p.Pro152Ala)	not specified [RCV004071397]	uncertain significance	17	7855688	7855688	Human		name
155917620	CV2236608	single nucleotide variant	NM_203411.2(TMEM88):c.464G>T (p.Gly155Val)	not specified [RCV004110591]	uncertain significance	17	7855698	7855698	Human		name
155959841	CV2252618	single nucleotide variant	NM_203411.2(TMEM88):c.394C>T (p.Arg132Trp)	not specified [RCV004118494]	uncertain significance	17	7855628	7855628	Human		name
155903117	CV2353523	single nucleotide variant	NM_203411.2(TMEM88):c.332G>A (p.Arg111His)	not specified [RCV004199507]	uncertain significance	17	7855566	7855566	Human		name
156081524	CV2368810	single nucleotide variant	NM_203411.2(TMEM88):c.451G>A (p.Val151Ile)	not specified [RCV004214686]	uncertain significance	17	7855685	7855685	Human		name
401721286	CV2673664	single nucleotide variant	NM_203411.2(TMEM88):c.383G>A (p.Arg128Gln)	not specified [RCV004282395]	uncertain significance	17	7855617	7855617	Human		name
405772468	CV3343303	single nucleotide variant	NM_203411.2(TMEM88):c.388C>G (p.Leu130Val)	not specified [RCV004470530]	uncertain significance	17	7855622	7855622	Human		name
405772473	CV3343304	single nucleotide variant	NM_203411.2(TMEM88):c.403C>A (p.Arg135Ser)	not specified [RCV004470531]	uncertain significance	17	7855637	7855637	Human		name
407526998	CV3482857	single nucleotide variant	NM_203411.2(TMEM88):c.316G>A (p.Ala106Thr)	not specified [RCV004679845]	uncertain significance	17	7855550	7855550	Human		name
597800757	CV3610731	single nucleotide variant	NM_001146685.2(TMEM88B):c.9G>T (p.Glu3Asp)	not specified [RCV004880378]	uncertain significance	1	1426136	1426136	Human		name
407527008	CV3482860	single nucleotide variant	NM_001146685.2(TMEM88B):c.47G>C (p.Gly16Ala)	not specified [RCV004679848]	uncertain significance	1	1426174	1426174	Human		name
597800749	CV3610727	single nucleotide variant	NM_001146685.2(TMEM88B):c.55G>A (p.Asp19Asn)	not specified [RCV004880374]	uncertain significance	1	1426182	1426182	Human		name
597800753	CV3610729	single nucleotide variant	NM_001146685.2(TMEM88B):c.77G>A (p.Arg26Gln)	not specified [RCV004880376]	uncertain significance	1	1426204	1426204	Human		name
597800751	CV3610728	single nucleotide variant	NM_001146685.2(TMEM88B):c.131C>A (p.Pro44His)	not specified [RCV004880375]	uncertain significance	1	1426258	1426258	Human		name
597800755	CV3610730	single nucleotide variant	NM_001146685.2(TMEM88B):c.215C>T (p.Pro72Leu)	not specified [RCV004880377]	uncertain significance	1	1426342	1426342	Human		name
597800759	CV3610732	single nucleotide variant	NM_001146685.2(TMEM88B):c.254C>T (p.Ser85Leu)	not specified [RCV004880379]	uncertain significance	1	1426381	1426381	Human		name
597800768	CV3610736	single nucleotide variant	NM_001146685.2(TMEM88B):c.292C>G (p.Leu98Val)	not specified [RCV004880383]	uncertain significance	1	1427587	1427587	Human		name
407527001	CV3482858	single nucleotide variant	NM_001146685.2(TMEM88B):c.379G>T (p.Ala127Ser)	not specified [RCV004679846]	uncertain significance	1	1427674	1427674	Human		name
407527004	CV3482859	single nucleotide variant	NM_001146685.2(TMEM88B):c.313G>C (p.Ala105Pro)	not specified [RCV004679847]	uncertain significance	1	1427608	1427608	Human		name
597800763	CV3610734	single nucleotide variant	NM_001146685.2(TMEM88B):c.401G>T (p.Arg134Leu)	not specified [RCV004880381]	uncertain significance	1	1427696	1427696	Human		name
597800765	CV3610735	single nucleotide variant	NM_001146685.2(TMEM88B):c.401G>A (p.Arg134His)	not specified [RCV004880382]	uncertain significance	1	1427696	1427696	Human		name

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