Anapc7 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

35 records found for search term Anapc7

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156257616	CV2219907	single nucleotide variant	NM_016238.3(ANAPC7):c.-72T>G	not specified [RCV004095535]	uncertain significance	12	110403699	110403699	Human		name
156276748	CV2351962	single nucleotide variant	NM_016238.3(ANAPC7):c.-57C>G	not specified [RCV004191067]	uncertain significance	12	110403684	110403684	Human		name
405817494	CV3283746	single nucleotide variant	NM_016238.3(ANAPC7):c.-56T>A	not specified [RCV004412404]	uncertain significance	12	110403683	110403683	Human		name
405817484	CV3283756	single nucleotide variant	NM_016238.3(ANAPC7):c.-23T>A	not specified [RCV004412414]	uncertain significance	12	110403650	110403650	Human		name
407474103	CV3453528	single nucleotide variant	NM_016238.3(ANAPC7):c.-57C>T	not specified [RCV004638056]	likely benign	12	110403684	110403684	Human		name
407474266	CV3453553	single nucleotide variant	NM_016238.3(ANAPC7):c.-14C>T	not specified [RCV004638075]	uncertain significance	12	110403641	110403641	Human		name
597632625	CV3698949	single nucleotide variant	NM_016238.3(ANAPC7):c.-72T>A	not specified [RCV004940057]	uncertain significance	12	110403699	110403699	Human		name
151348436	CV1325033	deletion	NM_016238.3(ANAPC7):c.409-2478_818-89del	Ferguson-Bonni neurodevelopmental syndrome [RCV001812627]	pathogenic	12	110383049	110391101	Human	1	name
156099016	CV2367335	single nucleotide variant	NM_016238.3(ANAPC7):c.37G>T (p.Ala13Ser)	not specified [RCV004209243]	uncertain significance	12	110403591	110403591	Human		name
598234489	CV3980075	single nucleotide variant	NM_016238.3(ANAPC7):c.38C>T (p.Ala13Val)	not specified [RCV005363516]	uncertain significance	12	110403590	110403590	Human		name
243051547	CV2415920	single nucleotide variant	NM_016238.3(ANAPC7):c.137T>C (p.Leu46Ser)	Ferguson-Bonni neurodevelopmental syndrome [RCV003148540]	uncertain significance	12	110396417	110396417	Human	1	name
405689985	CV3227321	deletion	NM_016238.3(ANAPC7):c.493del (p.Cys165fs)	Ferguson-Bonni neurodevelopmental syndrome [RCV003991665]	uncertain significance	12	110388539	110388539	Human	1	name
407474222	CV3453538	single nucleotide variant	NM_016238.3(ANAPC7):c.155C>G (p.Ser52Cys)	not specified [RCV004638063]	uncertain significance	12	110396399	110396399	Human		name
407474239	CV3453544	single nucleotide variant	NM_016238.3(ANAPC7):c.292C>A (p.Leu98Ile)	not specified [RCV004638068]	uncertain significance	12	110395217	110395217	Human		name
155915954	CV2200609	single nucleotide variant	NM_016238.3(ANAPC7):c.722G>A (p.Gly241Glu)	not specified [RCV004078948]	uncertain significance	12	110386422	110386422	Human		name
156169008	CV2247286	single nucleotide variant	NM_016238.3(ANAPC7):c.865G>A (p.Asp289Asn)	not specified [RCV004115062]	uncertain significance	12	110382913	110382913	Human		name
401872200	CV2779581	single nucleotide variant	NM_016238.3(ANAPC7):c.830A>G (p.Tyr277Cys)	not specified [RCV004351294]	uncertain significance	12	110382948	110382948	Human		name
405817489	CV3283751	single nucleotide variant	NM_016238.3(ANAPC7):c.454C>A (p.Arg152Ser)	not specified [RCV004412409]	uncertain significance	12	110388578	110388578	Human		name
597795613	CV3698944	single nucleotide variant	NM_016238.3(ANAPC7):c.368C>T (p.Ala123Val)	not specified [RCV004934911]	uncertain significance	12	110395141	110395141	Human		name
597632617	CV3698947	single nucleotide variant	NM_016238.3(ANAPC7):c.799G>C (p.Asp267His)	not specified [RCV004940055]	uncertain significance	12	110386345	110386345	Human		name
597632628	CV3698951	single nucleotide variant	NM_016238.3(ANAPC7):c.864G>C (p.Glu288Asp)	not specified [RCV004940058]	uncertain significance	12	110382914	110382914	Human		name
598234457	CV3980065	single nucleotide variant	NM_016238.3(ANAPC7):c.603G>C (p.Trp201Cys)	not specified [RCV005363512]	uncertain significance	12	110387810	110387810	Human		name
598234591	CV3980109	single nucleotide variant	NM_016238.3(ANAPC7):c.582A>C (p.Gln194His)	not specified [RCV005363531]	uncertain significance	12	110387831	110387831	Human		name
598259355	CV3980119	single nucleotide variant	NM_016238.3(ANAPC7):c.581A>C (p.Gln194Pro)	not specified [RCV005347401]	uncertain significance	12	110387832	110387832	Human		name
598234662	CV3980138	single nucleotide variant	NM_016238.3(ANAPC7):c.756C>G (p.Asp252Glu)	not specified [RCV005363541]	uncertain significance	12	110386388	110386388	Human		name
598234684	CV3980146	single nucleotide variant	NM_016238.3(ANAPC7):c.592A>T (p.Asn198Tyr)	not specified [RCV005363544]	uncertain significance	12	110387821	110387821	Human		name
156233137	CV2273883	single nucleotide variant	NM_016238.3(ANAPC7):c.1087C>T (p.Arg363Trp)	not specified [RCV004132506]	uncertain significance	12	110381797	110381797	Human		name
597632613	CV3698945	single nucleotide variant	NM_016238.3(ANAPC7):c.1402G>A (p.Ala468Thr)	not specified [RCV004940054]	uncertain significance	12	110376172	110376172	Human		name
597795616	CV3698946	single nucleotide variant	NM_016238.3(ANAPC7):c.1525C>G (p.Gln509Glu)	not specified [RCV004934912]	uncertain significance	12	110374317	110374317	Human		name
597632620	CV3698948	single nucleotide variant	NM_016238.3(ANAPC7):c.1192A>G (p.Asn398Asp)	not specified [RCV004940056]	uncertain significance	12	110377558	110377558	Human		name
597632632	CV3698952	single nucleotide variant	NM_016238.3(ANAPC7):c.1621G>A (p.Glu541Lys)	not specified [RCV004940059]	uncertain significance	12	110374221	110374221	Human		name
598259296	CV3980088	single nucleotide variant	NM_016238.3(ANAPC7):c.1459G>A (p.Ala487Thr)	not specified [RCV005347389]	uncertain significance	12	110376115	110376115	Human		name
598212662	CV3980098	single nucleotide variant	NM_016238.3(ANAPC7):c.1219G>A (p.Ala407Thr)	not specified [RCV005358856]	uncertain significance	12	110377531	110377531	Human		name
598234642	CV3980128	single nucleotide variant	NM_016238.3(ANAPC7):c.1005C>G (p.Asn335Lys)	not specified [RCV005363538]	uncertain significance	12	110381879	110381879	Human		name
401932356	CV2816827	microsatellite	NM_016238.3(ANAPC7):c.159_160del (p.Phe54fs)	not provided [RCV003391998]	uncertain significance	12	110396394	110396395	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