Tal1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

46 records found for search term Tal1

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8629577	CV84724	single nucleotide variant	NM_003189.5(TAL1):c.*282G>A	Malignant melanoma [RCV000064806]	not provided	1	47219438	47219438	Human		name
150487838	CV1237394	single nucleotide variant	NM_001290403.2(TAL1):c.447-72G>C	not provided [RCV001654243]	benign	1	47224170	47224170	Human		name
150452697	CV1276759	single nucleotide variant	NM_001290403.2(TAL1):c.446+123G>C	not provided [RCV001708549]	benign	1	47225320	47225320	Human		name
150448758	CV1253597	microsatellite	NM_001290403.2(TAL1):c.-1-19TCTG[2]	not provided [RCV001667525]	benign	1	47225897	47225900	Human		name
155951730	CV2264139	single nucleotide variant	NM_001290403.2(TAL1):c.88C>G (p.His30Asp)	not specified [RCV004136295]	uncertain significance	1	47225801	47225801	Human		name
155917708	CV2332866	single nucleotide variant	NM_001290403.2(TAL1):c.31C>T (p.Arg11Cys)	not specified [RCV004192129]	uncertain significance	1	47225858	47225858	Human		name
156212432	CV2366949	single nucleotide variant	NM_001290403.2(TAL1):c.64G>A (p.Ala22Thr)	not specified [RCV004213355]	uncertain significance	1	47225825	47225825	Human		name
405276900	CV3198698	single nucleotide variant	NM_001290403.2(TAL1):c.792T>G (p.Ala264=)	TAL1-related disorder [RCV003904024]	likely benign	1	47219924	47219924	Human		name , trait , alternate_id
405266652	CV3202051	single nucleotide variant	NM_001290403.2(TAL1):c.795T>G (p.Gly265=)	TAL1-related disorder [RCV003911533]	benign	1	47219921	47219921	Human		name , trait , alternate_id
405270169	CV3215394	single nucleotide variant	NM_001290403.2(TAL1):c.486C>G (p.Thr162=)	TAL1-related disorder [RCV003949146]	likely benign	1	47224059	47224059	Human		name , trait , alternate_id
405262017	CV3216519	single nucleotide variant	NM_001290403.2(TAL1):c.813A>C (p.Gly271=)	TAL1-related disorder [RCV003944649]	likely benign	1	47219903	47219903	Human		name , trait , alternate_id
405278739	CV3216771	single nucleotide variant	NM_001290403.2(TAL1):c.80C>G (p.Ala27Gly)	TAL1-related disorder [RCV003954643]	likely benign	1	47225809	47225809	Human		name , trait , alternate_id
405278965	CV3220519	single nucleotide variant	NM_001290403.2(TAL1):c.819C>T (p.Gly273=)	TAL1-related disorder [RCV003976701]	benign	1	47219897	47219897	Human		name , trait , alternate_id
15156572	CV707448	single nucleotide variant	NM_001290403.2(TAL1):c.441C>G (p.Leu147=)	not provided [RCV000969138]	likely benign	1	47225448	47225448	Human		name
15188088	CV762002	single nucleotide variant	NM_001290403.2(TAL1):c.519C>T (p.Pro173=)	not provided [RCV000931848]	likely benign	1	47224026	47224026	Human		name
156242691	CV2262143	single nucleotide variant	NM_001290403.2(TAL1):c.212C>T (p.Ala71Val)	not specified [RCV004126592]	uncertain significance	1	47225677	47225677	Human		name
156103252	CV2291591	single nucleotide variant	NM_001290403.2(TAL1):c.166G>T (p.Ala56Ser)	not specified [RCV004155888]	uncertain significance	1	47225723	47225723	Human		name
156332376	CV2339773	single nucleotide variant	NM_001290403.2(TAL1):c.262G>A (p.Val88Met)	not specified [RCV004196471]	uncertain significance	1	47225627	47225627	Human		name
329396163	CV2451930	single nucleotide variant	NM_001290403.2(TAL1):c.211G>C (p.Ala71Pro)	not specified [RCV004276598]	uncertain significance	1	47225678	47225678	Human		name
405272621	CV3210099	single nucleotide variant	NM_001290403.2(TAL1):c.184G>C (p.Gly62Arg)	TAL1-related disorder [RCV003914348]	likely benign	1	47225705	47225705	Human		name , trait , alternate_id
407506600	CV3475145	single nucleotide variant	NM_001290403.2(TAL1):c.257A>G (p.His86Arg)	not specified [RCV004671173]	uncertain significance	1	47225632	47225632	Human		name
597748707	CV3612229	single nucleotide variant	NM_001290403.2(TAL1):c.247G>A (p.Glu83Lys)	not specified [RCV004866318]	uncertain significance	1	47225642	47225642	Human		name
597748726	CV3612234	single nucleotide variant	NM_001290403.2(TAL1):c.274G>A (p.Glu92Lys)	not specified [RCV004866322]	uncertain significance	1	47225615	47225615	Human		name
156268979	CV2305820	single nucleotide variant	NM_001290403.2(TAL1):c.799G>A (p.Gly267Ser)	not specified [RCV004167623]	uncertain significance	1	47219917	47219917	Human		name
156071337	CV2337750	single nucleotide variant	NM_001290403.2(TAL1):c.925G>T (p.Ala309Ser)	not specified [RCV004183771]	uncertain significance	1	47219791	47219791	Human		name
155902850	CV2356540	single nucleotide variant	NM_001290403.2(TAL1):c.392C>T (p.Ala131Val)	not specified [RCV004199450]	uncertain significance	1	47225497	47225497	Human		name
155917010	CV2366807	single nucleotide variant	NM_001290403.2(TAL1):c.805G>A (p.Gly269Ser)	not specified [RCV004210797]	uncertain significance	1	47219911	47219911	Human		name
155909079	CV2369412	single nucleotide variant	NM_001290403.2(TAL1):c.488C>T (p.Thr163Ile)	not specified [RCV004210358]	uncertain significance	1	47224057	47224057	Human		name
156156212	CV2393438	single nucleotide variant	NM_001290403.2(TAL1):c.383C>A (p.Ala128Asp)	not specified [RCV004228933]	uncertain significance	1	47225506	47225506	Human		name
329358073	CV2427934	single nucleotide variant	NM_001290403.2(TAL1):c.395C>G (p.Pro132Arg)	not specified [RCV004254322]	uncertain significance	1	47225494	47225494	Human		name
401772841	CV2708977	single nucleotide variant	NM_001290403.2(TAL1):c.340G>A (p.Gly114Ser)	not specified [RCV004314337]	uncertain significance	1	47225549	47225549	Human		name
401866327	CV2782829	single nucleotide variant	NM_001290403.2(TAL1):c.849C>G (p.Asp283Glu)	not specified [RCV004361641]	uncertain significance	1	47219867	47219867	Human		name
405273126	CV3210371	single nucleotide variant	NM_001290403.2(TAL1):c.310G>T (p.Ala104Ser)	TAL1-related disorder [RCV003914593]	likely benign	1	47225579	47225579	Human		name , trait , alternate_id
405284297	CV3213698	single nucleotide variant	NM_001290403.2(TAL1):c.311C>T (p.Ala104Val)	TAL1-related disorder [RCV003922258]	likely benign	1	47225578	47225578	Human		name , trait , alternate_id
405762997	CV3327713	single nucleotide variant	NM_001290403.2(TAL1):c.533T>C (p.Ile178Thr)	not specified [RCV004468957]	uncertain significance	1	47224012	47224012	Human		name
405763005	CV3327714	single nucleotide variant	NM_001290403.2(TAL1):c.800G>A (p.Gly267Asp)	not specified [RCV004468958]	uncertain significance	1	47219916	47219916	Human		name
405763008	CV3327715	single nucleotide variant	NM_001290403.2(TAL1):c.929C>T (p.Pro310Leu)	not specified [RCV004468959]	uncertain significance	1	47219787	47219787	Human		name
407506597	CV3475144	single nucleotide variant	NM_001290403.2(TAL1):c.878G>C (p.Ser293Thr)	not specified [RCV004671172]	uncertain significance	1	47219838	47219838	Human		name
407506604	CV3475146	single nucleotide variant	NM_001290403.2(TAL1):c.308C>G (p.Pro103Arg)	not specified [RCV004671174]	uncertain significance	1	47225581	47225581	Human		name
407530483	CV3475147	single nucleotide variant	NM_001290403.2(TAL1):c.863A>G (p.Asn288Ser)	not specified [RCV004681933]	uncertain significance	1	47219853	47219853	Human		name
407530486	CV3475148	single nucleotide variant	NM_001290403.2(TAL1):c.329C>T (p.Ala110Val)	not specified [RCV004681934]	uncertain significance	1	47225560	47225560	Human		name
597748702	CV3612228	single nucleotide variant	NM_001290403.2(TAL1):c.821G>A (p.Gly274Asp)	not specified [RCV004866317]	uncertain significance	1	47219895	47219895	Human		name
597748715	CV3612232	single nucleotide variant	NM_001290403.2(TAL1):c.515C>A (p.Ser172Tyr)	not specified [RCV004866320]	uncertain significance	1	47224030	47224030	Human		name
597748720	CV3612233	single nucleotide variant	NM_001290403.2(TAL1):c.850G>A (p.Val284Met)	not specified [RCV004866321]	uncertain significance	1	47219866	47219866	Human		name
597748731	CV3612235	single nucleotide variant	NM_001290403.2(TAL1):c.763A>G (p.Lys255Glu)	not specified [RCV004866323]	uncertain significance	1	47219953	47219953	Human		name
598182594	CV3920022	single nucleotide variant	NM_001290403.2(TAL1):c.354G>A (p.Met118Ile)	not specified [RCV005286966]	uncertain significance	1	47225535	47225535	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