Tomm20 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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24 records found for search term Tomm20

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150331129	CV1170690	single nucleotide variant	NM_014765.3(TOMM20):c.*2185A>G	not provided [RCV001538498]	benign	1	235109879	235109879	Human		name
597786591	CV3614313	single nucleotide variant	NM_014765.3(TOMM20):c.104A>G (p.Lys35Arg)	not specified [RCV004875383]	uncertain significance	1	235128612	235128612	Human		name
597786594	CV3614314	single nucleotide variant	NM_014765.3(TOMM20):c.115C>G (p.Arg39Gly)	not specified [RCV004875384]	uncertain significance	1	235128601	235128601	Human		name
598187886	CV3928032	single nucleotide variant	NM_014765.3(TOMM20):c.124A>G (p.Arg42Gly)	not specified [RCV005287851]	uncertain significance	1	235122370	235122370	Human		name
329396780	CV2455785	single nucleotide variant	NM_014765.3(TOMM20):c.425A>G (p.Asp142Gly)	not specified [RCV004279077]	uncertain significance	1	235112077	235112077	Human		name
598187881	CV3928031	single nucleotide variant	NM_014765.3(TOMM20):c.400G>A (p.Val134Ile)	not specified [RCV005287850]	uncertain significance	1	235112102	235112102	Human		name
156367784	CV2266877	single nucleotide variant	NM_207377.3(TOMM20L):c.25C>G (p.Arg9Gly)	not specified [RCV004131544]	likely benign	14	58395982	58395982	Human		name
405757122	CV3346895	single nucleotide variant	NM_207377.3(TOMM20L):c.66C>G (p.Phe22Leu)	not specified [RCV004467995]	uncertain significance	14	58396023	58396023	Human		name
407531580	CV3486728	single nucleotide variant	NM_207377.3(TOMM20L):c.88A>G (p.Asn30Asp)	not specified [RCV004682566]	likely benign	14	58396045	58396045	Human		name
156056375	CV2243297	single nucleotide variant	NM_207377.3(TOMM20L):c.280A>T (p.Ile94Phe)	not specified [RCV004110175]	uncertain significance	14	58407343	58407343	Human		name
156276919	CV2255853	single nucleotide variant	NM_207377.3(TOMM20L):c.100C>G (p.Arg34Gly)	not specified [RCV004122012]	uncertain significance	14	58396057	58396057	Human		name
156064167	CV2272412	single nucleotide variant	NM_207377.3(TOMM20L):c.143G>A (p.Arg48Lys)	not specified [RCV004133334]	uncertain significance	14	58396304	58396304	Human		name
155921639	CV2350702	single nucleotide variant	NM_207377.3(TOMM20L):c.104G>A (p.Gly35Glu)	not specified [RCV004207051]	uncertain significance	14	58396061	58396061	Human		name
156337625	CV2370463	single nucleotide variant	NM_207377.3(TOMM20L):c.235C>T (p.Arg79Trp)	not specified [RCV004215812]	uncertain significance	14	58402734	58402734	Human		name
401760969	CV2695229	single nucleotide variant	NM_207377.3(TOMM20L):c.196A>G (p.Lys66Glu)	not specified [RCV004303364]	uncertain significance	14	58402695	58402695	Human		name
407531582	CV3486729	single nucleotide variant	NM_207377.3(TOMM20L):c.266A>C (p.Glu89Ala)	not specified [RCV004682567]	uncertain significance	14	58407329	58407329	Human		name
407461078	CV3486731	single nucleotide variant	NM_207377.3(TOMM20L):c.288C>A (p.His96Gln)	not specified [RCV004687563]	uncertain significance	14	58407351	58407351	Human		name
597786598	CV3614315	single nucleotide variant	NM_207377.3(TOMM20L):c.194C>T (p.Thr65Met)	not specified [RCV004875385]	uncertain significance	14	58402693	58402693	Human		name
598187892	CV3928033	single nucleotide variant	NM_207377.3(TOMM20L):c.205A>G (p.Lys69Glu)	not specified [RCV005287852]	uncertain significance	14	58402704	58402704	Human		name
156363243	CV2329758	single nucleotide variant	NM_207377.3(TOMM20L):c.313G>A (p.Glu105Lys)	not specified [RCV004183231]	uncertain significance	14	58407376	58407376	Human		name
401865400	CV2778741	single nucleotide variant	NM_207377.3(TOMM20L):c.451C>A (p.Pro151Thr)	not specified [RCV004346650]	uncertain significance	14	58408574	58408574	Human		name
407531584	CV3486730	single nucleotide variant	NM_207377.3(TOMM20L):c.387A>T (p.Lys129Asn)	not specified [RCV004682568]	uncertain significance	14	58407450	58407450	Human		name
597786602	CV3614316	single nucleotide variant	NM_207377.3(TOMM20L):c.426T>A (p.Asn142Lys)	not specified [RCV004875386]	uncertain significance	14	58408549	58408549	Human		name
597786608	CV3614317	single nucleotide variant	NM_207377.3(TOMM20L):c.355C>T (p.Pro119Ser)	not specified [RCV004875387]	uncertain significance	14	58407418	58407418	Human		name

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