Ccdc85c Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

48 records found for search term Ccdc85c

Refine Term:

Sort By:

Export

CSV

TAB

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

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message