Idi2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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33 records found for search term Idi2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155929723	CV2278270	single nucleotide variant	NM_033261.3(IDI2):c.30C>G (p.Asp10Glu)	not specified [RCV004147580]	uncertain significance	10	1024694	1024694	Human		name
401867422	CV2773566	single nucleotide variant	NM_033261.3(IDI2):c.92T>C (p.Ile31Thr)	not specified [RCV004355974]	uncertain significance	10	1024632	1024632	Human		name
405791692	CV3267310	single nucleotide variant	NM_033261.3(IDI2):c.94G>C (p.Gly32Arg)	not specified [RCV004399946]	uncertain significance	10	1024630	1024630	Human		name
597762579	CV3683082	single nucleotide variant	NM_033261.3(IDI2):c.76G>A (p.Glu26Lys)	not specified [RCV004926156]	uncertain significance	10	1024648	1024648	Human		name
8633477	CV88692	single nucleotide variant	NM_033261.2(IDI2):c.504G>A (p.Thr168=)	Malignant melanoma [RCV000068787]	not provided	10	1019697	1019697	Human		name
156256944	CV2307842	single nucleotide variant	NM_033261.3(IDI2):c.164G>A (p.Ser55Asn)	not specified [RCV004170304]	uncertain significance	10	1022754	1022754	Human		name
156069541	CV2353996	single nucleotide variant	NM_033261.3(IDI2):c.223G>A (p.Val75Ile)	not specified [RCV004204430]	likely benign	10	1022695	1022695	Human		name
156066100	CV2376147	single nucleotide variant	NM_033261.3(IDI2):c.155G>A (p.Arg52Gln)	not specified [RCV004220377]	uncertain significance	10	1022763	1022763	Human		name
401758877	CV2694325	single nucleotide variant	NM_033261.3(IDI2):c.151C>T (p.His51Tyr)	not specified [RCV004304519]	uncertain significance	10	1022767	1022767	Human		name
401895524	CV2774405	single nucleotide variant	NM_033261.3(IDI2):c.110G>A (p.Arg37Lys)	not specified [RCV004347745]	likely benign	10	1024614	1024614	Human		name
405791674	CV3267303	single nucleotide variant	NM_033261.3(IDI2):c.191G>A (p.Arg64Gln)	not specified [RCV004399939]	uncertain significance	10	1022727	1022727	Human		name
405791676	CV3267304	single nucleotide variant	NM_033261.3(IDI2):c.220A>G (p.Lys74Glu)	not specified [RCV004399940]	uncertain significance	10	1022698	1022698	Human		name
598257715	CV3979070	single nucleotide variant	NM_033261.3(IDI2):c.218C>T (p.Thr73Met)	not specified [RCV005347047]	uncertain significance	10	1022700	1022700	Human		name
155974214	CV2235657	single nucleotide variant	NM_033261.3(IDI2):c.609G>T (p.Arg203Ser)	not specified [RCV004111802]	uncertain significance	10	1019592	1019592	Human		name
156065640	CV2240308	single nucleotide variant	NM_033261.3(IDI2):c.627G>T (p.Trp209Cys)	not specified [RCV004112865]	uncertain significance	10	1019574	1019574	Human		name
156097408	CV2253183	single nucleotide variant	NM_033261.3(IDI2):c.599T>C (p.Ile200Thr)	not specified [RCV004120948]	uncertain significance	10	1019602	1019602	Human		name
156156681	CV2314399	single nucleotide variant	NM_033261.3(IDI2):c.555G>C (p.Arg185Ser)	not specified [RCV004168518]	uncertain significance	10	1019646	1019646	Human		name
329357730	CV2453765	single nucleotide variant	NM_033261.3(IDI2):c.479C>T (p.Thr160Ile)	not specified [RCV004269392]	uncertain significance	10	1019722	1019722	Human		name
401864200	CV2760846	single nucleotide variant	NM_033261.3(IDI2):c.305T>C (p.Ile102Thr)	not specified [RCV004336483]	uncertain significance	10	1020828	1020828	Human		name
401895600	CV2774491	single nucleotide variant	NM_033261.3(IDI2):c.310G>T (p.Val104Leu)	not specified [RCV004349982]	uncertain significance	10	1020823	1020823	Human		name
405791679	CV3267305	single nucleotide variant	NM_033261.3(IDI2):c.298G>C (p.Asp100His)	not specified [RCV004399941]	uncertain significance	10	1020835	1020835	Human		name
405791681	CV3267306	single nucleotide variant	NM_033261.3(IDI2):c.332G>A (p.Arg111His)	not specified [RCV004399942]	likely benign	10	1020801	1020801	Human		name
405791684	CV3267307	single nucleotide variant	NM_033261.3(IDI2):c.359G>C (p.Gly120Ala)	not specified [RCV004399943]	uncertain significance	10	1020774	1020774	Human		name
405791687	CV3267308	single nucleotide variant	NM_033261.3(IDI2):c.410A>T (p.Lys137Met)	not specified [RCV004399944]	uncertain significance	10	1019791	1019791	Human		name
405791689	CV3267309	single nucleotide variant	NM_033261.3(IDI2):c.620G>A (p.Arg207Gln)	not specified [RCV004399945]	uncertain significance	10	1019581	1019581	Human		name
407480405	CV3444434	single nucleotide variant	NM_033261.3(IDI2):c.650C>T (p.Pro217Leu)	not specified [RCV004635508]	uncertain significance	10	1019551	1019551	Human		name
597762569	CV3683080	single nucleotide variant	NM_033261.3(IDI2):c.581C>A (p.Thr194Asn)	not specified [RCV004926154]	uncertain significance	10	1019620	1019620	Human		name
597762574	CV3683081	single nucleotide variant	NM_033261.3(IDI2):c.436G>A (p.Glu146Lys)	not specified [RCV004926155]	uncertain significance	10	1019765	1019765	Human		name
597762582	CV3683083	single nucleotide variant	NM_033261.3(IDI2):c.589C>A (p.Leu197Ile)	not specified [RCV004926157]	uncertain significance	10	1019612	1019612	Human		name
597762586	CV3683084	single nucleotide variant	NM_033261.3(IDI2):c.390C>G (p.Phe130Leu)	not specified [RCV004926158]	uncertain significance	10	1019811	1019811	Human		name
597762591	CV3683085	single nucleotide variant	NM_033261.3(IDI2):c.493C>G (p.Pro165Ala)	not specified [RCV004926159]	uncertain significance	10	1019708	1019708	Human		name
598257710	CV3979068	single nucleotide variant	NM_033261.3(IDI2):c.331C>A (p.Arg111Ser)	not specified [RCV005347046]	uncertain significance	10	1020802	1020802	Human		name
598206376	CV3979069	single nucleotide variant	NM_033261.3(IDI2):c.350G>C (p.Gly117Ala)	not specified [RCV005337769]	uncertain significance	10	1020783	1020783	Human		name

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