Ccdc127 Variant Search Result - Rat Genome Database

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34 records found for search term Ccdc127

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156242488	CV2306554	single nucleotide variant	NM_145265.3(CCDC127):c.37C>T (p.Arg13Trp)	not specified [RCV004157162]	uncertain significance	5	216813	216813	Human		name
401727408	CV2680998	single nucleotide variant	NM_145265.3(CCDC127):c.53C>T (p.Ala18Val)	not specified [RCV004296066]	uncertain significance	5	216797	216797	Human		name
401770487	CV2715199	single nucleotide variant	NM_145265.3(CCDC127):c.38G>A (p.Arg13Gln)	not specified [RCV004324553]	uncertain significance	5	216812	216812	Human		name
597786791	CV3638051	single nucleotide variant	NM_145265.3(CCDC127):c.70A>G (p.Ser24Gly)	not specified [RCV004900987]	uncertain significance	5	216780	216780	Human		name
156068971	CV2292655	single nucleotide variant	NM_145265.3(CCDC127):c.164A>C (p.Glu55Ala)	not specified [RCV004154342]	uncertain significance	5	205916	205916	Human		name
155962943	CV2308216	single nucleotide variant	NM_145265.3(CCDC127):c.233T>C (p.Ile78Thr)	not specified [RCV004164717]	uncertain significance	5	205847	205847	Human		name
156150982	CV2394697	single nucleotide variant	NM_145265.3(CCDC127):c.173C>A (p.Ala58Asp)	not specified [RCV004234377]	uncertain significance	5	205907	205907	Human		name
401760697	CV2715904	single nucleotide variant	NM_145265.3(CCDC127):c.182G>A (p.Arg61Gln)	not specified [RCV004329011]	likely benign	5	205898	205898	Human		name
401782607	CV2719901	single nucleotide variant	NM_145265.3(CCDC127):c.100A>G (p.Met34Val)	not specified [RCV004329302]	uncertain significance	5	216750	216750	Human		name
401867797	CV2777360	single nucleotide variant	NM_145265.3(CCDC127):c.260A>G (p.Gln87Arg)	not specified [RCV004354369]	uncertain significance	5	205820	205820	Human		name
598177143	CV3946693	single nucleotide variant	NM_145265.3(CCDC127):c.242A>G (p.Asn81Ser)	not specified [RCV005310159]	uncertain significance	5	205838	205838	Human		name
156178311	CV2201583	single nucleotide variant	NM_145265.3(CCDC127):c.311A>T (p.Glu104Val)	not specified [RCV004080072]	uncertain significance	5	205769	205769	Human		name
156041367	CV2219564	single nucleotide variant	NM_145265.3(CCDC127):c.521G>A (p.Cys174Tyr)	not specified [RCV004095295]	uncertain significance	5	205559	205559	Human		name
156337683	CV2224839	single nucleotide variant	NM_145265.3(CCDC127):c.710A>G (p.Tyr237Cys)	not specified [RCV004092936]	uncertain significance	5	205370	205370	Human		name
156075582	CV2230152	single nucleotide variant	NM_145265.3(CCDC127):c.538C>T (p.Arg180Cys)	not specified [RCV004099794]	uncertain significance	5	205542	205542	Human		name
156264375	CV2289840	single nucleotide variant	NM_145265.3(CCDC127):c.574G>T (p.Val192Leu)	not specified [RCV004150506]	uncertain significance	5	205506	205506	Human		name
156069980	CV2295778	single nucleotide variant	NM_145265.3(CCDC127):c.647A>G (p.Asp216Gly)	not specified [RCV004151705]	uncertain significance	5	205433	205433	Human		name
156163396	CV2319627	single nucleotide variant	NM_145265.3(CCDC127):c.500C>T (p.Thr167Ile)	not specified [RCV004185174]	uncertain significance	5	205580	205580	Human		name
156189326	CV2342407	single nucleotide variant	NM_145265.3(CCDC127):c.586G>A (p.Val196Ile)	not specified [RCV004194019]	uncertain significance	5	205494	205494	Human		name
329363588	CV2471804	single nucleotide variant	NM_145265.3(CCDC127):c.352A>G (p.Lys118Glu)	not specified [RCV004280843]	uncertain significance	5	205728	205728	Human		name
401772093	CV2719529	single nucleotide variant	NM_145265.3(CCDC127):c.680A>G (p.Lys227Arg)	not specified [RCV004327215]	uncertain significance	5	205400	205400	Human		name
401894100	CV2770296	single nucleotide variant	NM_145265.3(CCDC127):c.580G>T (p.Ala194Ser)	not specified [RCV004356172]	uncertain significance	5	205500	205500	Human		name
405755055	CV3302842	single nucleotide variant	NM_145265.3(CCDC127):c.320T>C (p.Ile107Thr)	not specified [RCV004432702]	uncertain significance	5	205760	205760	Human		name
405755062	CV3302843	single nucleotide variant	NM_145265.3(CCDC127):c.394A>G (p.Arg132Gly)	not specified [RCV004432703]	uncertain significance	5	205686	205686	Human		name
405755067	CV3302844	single nucleotide variant	NM_145265.3(CCDC127):c.547C>T (p.Arg183Trp)	not specified [RCV004432704]	uncertain significance	5	205533	205533	Human		name
405755079	CV3302846	single nucleotide variant	NM_145265.3(CCDC127):c.736G>A (p.Glu246Lys)	not specified [RCV004432706]	uncertain significance	5	205344	205344	Human		name
407483294	CV3418222	single nucleotide variant	NM_145265.3(CCDC127):c.730G>A (p.Val244Ile)	not specified [RCV004602827]	likely benign	5	205350	205350	Human		name
407483300	CV3418223	single nucleotide variant	NM_145265.3(CCDC127):c.314C>T (p.Ala105Val)	not specified [RCV004602828]	uncertain significance	5	205766	205766	Human		name
407483306	CV3418224	single nucleotide variant	NM_145265.3(CCDC127):c.606C>G (p.Asp202Glu)	not specified [RCV004602829]	uncertain significance	5	205474	205474	Human		name
597786786	CV3638052	single nucleotide variant	NM_145265.3(CCDC127):c.757G>C (p.Val253Leu)	not specified [RCV004900988]	uncertain significance	5	205323	205323	Human		name
597786782	CV3638053	single nucleotide variant	NM_145265.3(CCDC127):c.531T>A (p.Phe177Leu)	not specified [RCV004900989]	likely benign	5	205549	205549	Human		name
597786778	CV3638054	single nucleotide variant	NM_145265.3(CCDC127):c.580G>A (p.Ala194Thr)	not specified [RCV004900990]	uncertain significance	5	205500	205500	Human		name
598177136	CV3946692	single nucleotide variant	NM_145265.3(CCDC127):c.371G>A (p.Arg124Gln)	not specified [RCV005310158]	uncertain significance	5	205709	205709	Human		name
598177150	CV3946694	single nucleotide variant	NM_145265.3(CCDC127):c.509A>G (p.Gln170Arg)	not specified [RCV005310160]	uncertain significance	5	205571	205571	Human		name

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