Mtch1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

22 records found for search term Mtch1

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8632040	CV87246	single nucleotide variant	NM_014341.2(MTCH1):c.594C>T (p.Thr198=)	Malignant melanoma [RCV000067337]	not provided	6	36977689	36977689	Human		name
156265694	CV2198682	single nucleotide variant	NM_001271641.2(MTCH1):c.5G>C (p.Gly2Ala)	not specified [RCV004075693]	uncertain significance	6	36986169	36986169	Human		name
155955968	CV2281869	single nucleotide variant	NM_001271641.2(MTCH1):c.20A>T (p.Glu7Val)	not specified [RCV004136867]	uncertain significance	6	36986154	36986154	Human		name
597638867	CV3564319	single nucleotide variant	NM_001271641.2(MTCH1):c.23T>C (p.Val8Ala)	not specified [RCV004825009]	uncertain significance	6	36986151	36986151	Human		name
598180696	CV3989860	single nucleotide variant	NM_001271641.2(MTCH1):c.19G>A (p.Glu7Lys)	not specified [RCV005372160]	uncertain significance	6	36986155	36986155	Human		name
156305026	CV2369307	single nucleotide variant	NM_001271641.2(MTCH1):c.47C>G (p.Ala16Gly)	not specified [RCV004208217]	uncertain significance	6	36986127	36986127	Human		name
329385670	CV2462173	single nucleotide variant	NM_001271641.2(MTCH1):c.76G>T (p.Ala26Ser)	not specified [RCV004266188]	uncertain significance	6	36986098	36986098	Human		name
401735486	CV2699280	single nucleotide variant	NM_001271641.2(MTCH1):c.28C>G (p.Pro10Ala)	not specified [RCV004305544]	uncertain significance	6	36986146	36986146	Human		name
401880243	CV2766174	single nucleotide variant	NM_001271641.2(MTCH1):c.43G>T (p.Gly15Cys)	not specified [RCV004340618]	uncertain significance	6	36986131	36986131	Human		name
156174579	CV2326956	single nucleotide variant	NM_001271641.2(MTCH1):c.134C>T (p.Pro45Leu)	not specified [RCV004176765]	uncertain significance	6	36986040	36986040	Human		name
405799728	CV3365347	single nucleotide variant	NM_001271641.2(MTCH1):c.292C>T (p.Pro98Ser)	not specified [RCV004508857]	uncertain significance	6	36985882	36985882	Human		name
407475821	CV3447357	single nucleotide variant	NM_001271641.2(MTCH1):c.211G>A (p.Gly71Ser)	not specified [RCV004638441]	uncertain significance	6	36985963	36985963	Human		name
597648538	CV3564317	single nucleotide variant	NM_001271641.2(MTCH1):c.214C>A (p.Leu72Met)	not specified [RCV004833363]	uncertain significance	6	36985960	36985960	Human		name
156305359	CV2252606	single nucleotide variant	NM_001271641.2(MTCH1):c.434A>G (p.Lys145Arg)	not specified [RCV004118482]	uncertain significance	6	36978584	36978584	Human		name
156161896	CV2319508	single nucleotide variant	NM_001271641.2(MTCH1):c.356C>T (p.Thr119Ile)	not specified [RCV004185079]	uncertain significance	6	36981638	36981638	Human		name
401762294	CV2723389	single nucleotide variant	NM_001271641.2(MTCH1):c.979C>T (p.Pro327Ser)	not specified [RCV004329596]	uncertain significance	6	36970449	36970449	Human		name
405799775	CV3365362	single nucleotide variant	NM_001271641.2(MTCH1):c.713G>T (p.Ser238Ile)	not specified [RCV004508872]	uncertain significance	6	36975706	36975706	Human		name
405799802	CV3365371	single nucleotide variant	NM_001271641.2(MTCH1):c.833A>G (p.Asn278Ser)	not specified [RCV004508881]	uncertain significance	6	36972725	36972725	Human		name
597648548	CV3564318	single nucleotide variant	NM_001271641.2(MTCH1):c.383A>G (p.Tyr128Cys)	not specified [RCV004833364]	uncertain significance	6	36981611	36981611	Human		name
597638872	CV3564320	single nucleotide variant	NM_001271641.2(MTCH1):c.397T>C (p.Phe133Leu)	not specified [RCV004825010]	uncertain significance	6	36981597	36981597	Human		name
598214719	CV3989859	single nucleotide variant	NM_001271641.2(MTCH1):c.726G>T (p.Lys242Asn)	not specified [RCV005378621]	uncertain significance	6	36975693	36975693	Human		name
401747093	CV2679005	single nucleotide variant	NM_001271641.2(MTCH1):c.1092T>G (p.Ser364Arg)	not specified [RCV004295016]	uncertain significance	6	36970045	36970045	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