Ccdc85c Variant Search Result - Rat Genome Database

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48 records found for search term Ccdc85c

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156400849	CV2217303	single nucleotide variant	NM_001144995.2(CCDC85C):c.19A>C (p.Thr7Pro)	not specified [RCV004087743]	uncertain significance	14	99603941	99603941	Human		name
156283622	CV2360591	single nucleotide variant	NM_001144995.2(CCDC85C):c.41A>T (p.Glu14Val)	not specified [RCV004211348]	uncertain significance	14	99603919	99603919	Human		name
401902265	CV2807228	single nucleotide variant	NM_001144995.2(CCDC85C):c.891C>T (p.Arg297=)	not provided [RCV003393603]	likely benign	14	99522217	99522217	Human		name
405718474	CV3296109	single nucleotide variant	NM_001144995.2(CCDC85C):c.31G>T (p.Ala11Ser)	not specified [RCV004427828]	uncertain significance	14	99603929	99603929	Human		name
405718530	CV3296116	single nucleotide variant	NM_001144995.2(CCDC85C):c.95C>T (p.Ala32Val)	not specified [RCV004427835]	uncertain significance	14	99603865	99603865	Human		name
401902264	CV2807227	single nucleotide variant	NM_001144995.2(CCDC85C):c.1014C>A (p.Pro338=)	not provided [RCV003393602]	likely benign	14	99517145	99517145	Human		name
405718465	CV3296108	single nucleotide variant	NM_001144995.2(CCDC85C):c.245A>G (p.Gln82Arg)	not specified [RCV004427827]	uncertain significance	14	99603715	99603715	Human		name
407491134	CV3428422	single nucleotide variant	NM_001144995.2(CCDC85C):c.161G>A (p.Arg54His)	not specified [RCV004604646]	uncertain significance	14	99603799	99603799	Human		name
597761801	CV3641277	single nucleotide variant	NM_001144995.2(CCDC85C):c.266G>C (p.Cys89Ser)	not specified [RCV004895026]	uncertain significance	14	99603694	99603694	Human		name
597765005	CV3641282	single nucleotide variant	NM_001144995.2(CCDC85C):c.235G>A (p.Asp79Asn)	not specified [RCV004895762]	uncertain significance	14	99603725	99603725	Human		name
598192022	CV3943475	single nucleotide variant	NM_001144995.2(CCDC85C):c.257A>G (p.Glu86Gly)	not specified [RCV005312719]	uncertain significance	14	99603703	99603703	Human		name
156180680	CV2225968	single nucleotide variant	NM_001144995.2(CCDC85C):c.716A>G (p.Lys239Arg)	not specified [RCV004105133]	uncertain significance	14	99603244	99603244	Human		name
155923363	CV2251931	single nucleotide variant	NM_001144995.2(CCDC85C):c.320G>T (p.Arg107Leu)	not specified [RCV004119901]	uncertain significance	14	99603640	99603640	Human		name
156361232	CV2269196	single nucleotide variant	NM_001144995.2(CCDC85C):c.666C>A (p.His222Gln)	not specified [RCV004130356]	uncertain significance	14	99603294	99603294	Human		name
156279683	CV2297746	single nucleotide variant	NM_001144995.2(CCDC85C):c.989C>T (p.Pro330Leu)	not specified [RCV004155423]	uncertain significance	14	99517170	99517170	Human		name
156090038	CV2367124	single nucleotide variant	NM_001144995.2(CCDC85C):c.436G>A (p.Glu146Lys)	not specified [RCV004215566]	uncertain significance	14	99603524	99603524	Human		name
156307913	CV2369838	single nucleotide variant	NM_001144995.2(CCDC85C):c.671C>T (p.Pro224Leu)	not specified [RCV004208312]	uncertain significance	14	99603289	99603289	Human		name
329351750	CV2455258	single nucleotide variant	NM_001144995.2(CCDC85C):c.862G>T (p.Ala288Ser)	not specified [RCV004274775]	uncertain significance	14	99536020	99536020	Human		name
329361616	CV2455794	single nucleotide variant	NM_001144995.2(CCDC85C):c.995C>G (p.Pro332Arg)	not specified [RCV004279085]	uncertain significance	14	99517164	99517164	Human		name
329362970	CV2464865	single nucleotide variant	NM_001144995.2(CCDC85C):c.688C>G (p.Pro230Ala)	not specified [RCV004284807]	uncertain significance	14	99603272	99603272	Human		name
401767811	CV2677825	single nucleotide variant	NM_001144995.2(CCDC85C):c.991G>A (p.Ala331Thr)	not specified [RCV004294323]	uncertain significance	14	99517168	99517168	Human		name
401721691	CV2710108	single nucleotide variant	NM_001144995.2(CCDC85C):c.467C>T (p.Ala156Val)	not specified [RCV004315163]	uncertain significance	14	99603493	99603493	Human		name
401877191	CV2769368	single nucleotide variant	NM_001144995.2(CCDC85C):c.766C>T (p.His256Tyr)	not specified [RCV004357359]	uncertain significance	14	99603194	99603194	Human		name
405718481	CV3296110	single nucleotide variant	NM_001144995.2(CCDC85C):c.458A>G (p.Glu153Gly)	not specified [RCV004427829]	uncertain significance	14	99603502	99603502	Human		name
405718488	CV3296111	single nucleotide variant	NM_001144995.2(CCDC85C):c.511G>A (p.Gly171Arg)	not specified [RCV004427830]	uncertain significance	14	99603449	99603449	Human		name
405718498	CV3296112	single nucleotide variant	NM_001144995.2(CCDC85C):c.566C>A (p.Pro189Gln)	not specified [RCV004427831]	uncertain significance	14	99603394	99603394	Human		name
405718506	CV3296113	single nucleotide variant	NM_001144995.2(CCDC85C):c.674C>T (p.Pro225Leu)	not specified [RCV004427832]	uncertain significance	14	99603286	99603286	Human		name
405718515	CV3296114	single nucleotide variant	NM_001144995.2(CCDC85C):c.730C>T (p.Arg244Cys)	not specified [RCV004427833]	uncertain significance	14	99603230	99603230	Human		name
405718520	CV3296115	single nucleotide variant	NM_001144995.2(CCDC85C):c.893C>T (p.Thr298Met)	not specified [RCV004427834]	uncertain significance	14	99522215	99522215	Human		name
405718540	CV3296117	single nucleotide variant	NM_001144995.2(CCDC85C):c.980C>T (p.Pro327Leu)	not specified [RCV004427836]	likely benign	14	99517179	99517179	Human		name
407491131	CV3428421	single nucleotide variant	NM_001144995.2(CCDC85C):c.802T>G (p.Ser268Ala)	not specified [RCV004604645]	uncertain significance	14	99536080	99536080	Human		name
407491137	CV3428423	single nucleotide variant	NM_001144995.2(CCDC85C):c.596C>T (p.Ala199Val)	not specified [RCV004604647]	uncertain significance	14	99603364	99603364	Human		name
407491141	CV3428424	single nucleotide variant	NM_001144995.2(CCDC85C):c.934C>G (p.Leu312Val)	not specified [RCV004604648]	uncertain significance	14	99522174	99522174	Human		name
597761805	CV3641278	single nucleotide variant	NM_001144995.2(CCDC85C):c.862G>A (p.Ala288Thr)	not specified [RCV004895027]	uncertain significance	14	99536020	99536020	Human		name
597764996	CV3641280	single nucleotide variant	NM_001144995.2(CCDC85C):c.305C>T (p.Ala102Val)	not specified [RCV004895760]	uncertain significance	14	99603655	99603655	Human		name
597765001	CV3641281	single nucleotide variant	NM_001144995.2(CCDC85C):c.664C>G (p.His222Asp)	not specified [RCV004895761]	uncertain significance	14	99603296	99603296	Human		name
597765009	CV3641283	single nucleotide variant	NM_001144995.2(CCDC85C):c.703G>A (p.Ala235Thr)	not specified [RCV004895763]	uncertain significance	14	99603257	99603257	Human		name
597765013	CV3641284	single nucleotide variant	NM_001144995.2(CCDC85C):c.731G>C (p.Arg244Pro)	not specified [RCV004895764]	uncertain significance	14	99603229	99603229	Human		name
598192003	CV3943471	single nucleotide variant	NM_001144995.2(CCDC85C):c.923C>T (p.Ser308Leu)	not specified [RCV005312716]	uncertain significance	14	99522185	99522185	Human		name
598192009	CV3943472	single nucleotide variant	NM_001144995.2(CCDC85C):c.956A>G (p.Tyr319Cys)	not specified [RCV005312717]	uncertain significance	14	99522152	99522152	Human		name
598228034	CV3943474	single nucleotide variant	NM_001144995.2(CCDC85C):c.416G>T (p.Arg139Leu)	not specified [RCV005319020]	uncertain significance	14	99603544	99603544	Human		name
598192027	CV3943476	single nucleotide variant	NM_001144995.2(CCDC85C):c.773G>A (p.Ser258Asn)	not specified [RCV005312720]	uncertain significance	14	99603187	99603187	Human		name
155986804	CV2363719	single nucleotide variant	NM_001144995.2(CCDC85C):c.1219C>T (p.Arg407Trp)	not specified [RCV004216663]	uncertain significance	14	99515287	99515287	Human		name
156251422	CV2394306	single nucleotide variant	NM_001144995.2(CCDC85C):c.1125G>T (p.Glu375Asp)	not specified [RCV004238529]	uncertain significance	14	99516233	99516233	Human		name
401773796	CV2702439	single nucleotide variant	NM_001144995.2(CCDC85C):c.1232C>T (p.Ser411Phe)	not specified [RCV004316952]	uncertain significance	14	99515274	99515274	Human		name
405718445	CV3296106	single nucleotide variant	NM_001144995.2(CCDC85C):c.1115G>T (p.Ser372Ile)	not specified [RCV004427825]	uncertain significance	14	99516243	99516243	Human		name
405718455	CV3296107	single nucleotide variant	NM_001144995.2(CCDC85C):c.1252C>T (p.Pro418Ser)	not specified [RCV004427826]	uncertain significance	14	99515254	99515254	Human		name
407491128	CV3428420	single nucleotide variant	NM_001144995.2(CCDC85C):c.1246A>C (p.Lys416Gln)	not specified [RCV004604644]	uncertain significance	14	99515260	99515260	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
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