Hoxc4 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

23 records found for search term Hoxc4

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8654050	CV130625	single nucleotide variant	NM_014620.5(HOXC4):c.-123-12551C>A	Lung cancer [RCV000111112]	uncertain significance	12	54040609	54040609	Human		name
407528101	CV3433825	single nucleotide variant	NM_153633.3(HOXC4):c.14C>G (p.Ser5Trp)	not specified [RCV004633026]	uncertain significance	12	54053936	54053936	Human		name
156190679	CV2289283	single nucleotide variant	NM_153633.3(HOXC4):c.83A>G (p.Tyr28Cys)	not specified [RCV004152265]	uncertain significance	12	54054005	54054005	Human		name
329370774	CV2461857	single nucleotide variant	NM_153633.3(HOXC4):c.77A>G (p.Asn26Ser)	not specified [RCV004271769]	uncertain significance	12	54053999	54053999	Human		name
401932187	CV2807059	single nucleotide variant	NM_153633.3(HOXC4):c.369C>T (p.Asp123=)	not provided [RCV003391863]	likely benign	12	54054291	54054291	Human		name
401932189	CV2807060	single nucleotide variant	NM_153633.3(HOXC4):c.387C>A (p.Ala129=)	not provided [RCV003391864]	likely benign	12	54054309	54054309	Human		name
156148013	CV2292623	single nucleotide variant	NM_153633.3(HOXC4):c.284A>G (p.Gln95Arg)	not specified [RCV004154313]	uncertain significance	12	54054206	54054206	Human		name
156164573	CV2319718	single nucleotide variant	NM_153633.3(HOXC4):c.257C>T (p.Ala86Val)	not specified [RCV004187255]	uncertain significance	12	54054179	54054179	Human		name
405797912	CV3263425	single nucleotide variant	NM_153633.3(HOXC4):c.271C>T (p.Pro91Ser)	not specified [RCV004402064]	uncertain significance	12	54054193	54054193	Human		name
597772686	CV3679719	single nucleotide variant	NM_153633.3(HOXC4):c.164C>G (p.Pro55Arg)	not specified [RCV004928731]	uncertain significance	12	54054086	54054086	Human		name
156072533	CV2325337	single nucleotide variant	NM_153633.3(HOXC4):c.692C>A (p.Ala231Glu)	not specified [RCV004177719]	uncertain significance	12	54055102	54055102	Human		name
401864775	CV2778038	single nucleotide variant	NM_153633.3(HOXC4):c.643C>A (p.His215Asn)	not specified [RCV004347992]	uncertain significance	12	54055053	54055053	Human		name
405798287	CV3263427	single nucleotide variant	NM_153633.3(HOXC4):c.653C>T (p.Pro218Leu)	not specified [RCV004402066]	uncertain significance	12	54055063	54055063	Human		name
405798282	CV3263428	single nucleotide variant	NM_153633.3(HOXC4):c.676C>A (p.Pro226Thr)	not specified [RCV004402067]	uncertain significance	12	54055086	54055086	Human		name
405798277	CV3263429	single nucleotide variant	NM_153633.3(HOXC4):c.748G>A (p.Ala250Thr)	not specified [RCV004402068]	uncertain significance	12	54055158	54055158	Human		name
405798273	CV3263430	single nucleotide variant	NM_153633.3(HOXC4):c.764A>G (p.Gln255Arg)	not specified [RCV004402069]	uncertain significance	12	54055174	54055174	Human		name
597772692	CV3679720	single nucleotide variant	NM_153633.3(HOXC4):c.299C>T (p.Pro100Leu)	not specified [RCV004928732]	uncertain significance	12	54054221	54054221	Human		name
597772695	CV3679721	single nucleotide variant	NM_153633.3(HOXC4):c.755C>T (p.Pro252Leu)	not specified [RCV004928733]	uncertain significance	12	54055165	54055165	Human		name
597772699	CV3679722	single nucleotide variant	NM_153633.3(HOXC4):c.322G>T (p.Ala108Ser)	not specified [RCV004928734]	uncertain significance	12	54054244	54054244	Human		name
598192012	CV3971778	single nucleotide variant	NM_153633.3(HOXC4):c.785C>T (p.Thr262Ile)	not specified [RCV005354380]	uncertain significance	12	54055195	54055195	Human		name
598192019	CV3971779	single nucleotide variant	NM_153633.3(HOXC4):c.718C>G (p.Pro240Ala)	not specified [RCV005354381]	uncertain significance	12	54055128	54055128	Human		name
598249266	CV3971780	single nucleotide variant	NM_153633.3(HOXC4):c.591G>C (p.Glu197Asp)	not specified [RCV005345562]	uncertain significance	12	54055001	54055001	Human		name
598249274	CV3971781	single nucleotide variant	NM_153633.3(HOXC4):c.491C>A (p.Thr164Asn)	not specified [RCV005345563]	uncertain significance	12	54054901	54054901	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