Sntg1 Variant Search Result - Rat Genome Database

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77 records found for search term Sntg1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405274430	CV3208804	single nucleotide variant	NM_018967.5(SNTG1):c.*4A>G	SNTG1-related disorder [RCV003951607]	likely benign	8	50792833	50792833	Human		name , trait , alternate_id
408367048	CV3511628	single nucleotide variant	NM_018967.5(SNTG1):c.364-5T>C	SNTG1-related disorder [RCV004757748]	likely benign	8	50502773	50502773	Human		name , trait , alternate_id
15197938	CV777943	single nucleotide variant	NM_018967.5(SNTG1):c.967-3A>C	not provided [RCV000956607]	benign	8	50658589	50658589	Human		name
405272760	CV3210199	duplication	NM_018967.5(SNTG1):c.1285-6dup	SNTG1-related disorder [RCV003914436]	benign	8	50751989	50751990	Human		name , trait , alternate_id
405262309	CV3213006	single nucleotide variant	NM_018967.5(SNTG1):c.1191+3G>T	SNTG1-related disorder [RCV003944782]	likely benign	8	50704755	50704755	Human		name , trait , alternate_id
405265260	CV3195586	single nucleotide variant	NM_018967.5(SNTG1):c.1284+25G>T	SNTG1-related disorder [RCV003897328]	benign	8	50709003	50709003	Human		name , trait , alternate_id
405291595	CV3205895	single nucleotide variant	NM_018967.5(SNTG1):c.1284+31T>C	SNTG1-related disorder [RCV003964010]	likely benign	8	50709009	50709009	Human		name , trait , alternate_id
401924001	CV2821079	single nucleotide variant	NM_018967.5(SNTG1):c.1192-979A>G	not provided [RCV003435487]	benign	8	50707907	50707907	Human		name
8650388	CV126963	single nucleotide variant	NM_001287813.1(SNTG1):c.811-681A>T	Lung cancer [RCV000107450]	uncertain significance	8	50590198	50590198	Human		name
8650384	CV126959	single nucleotide variant	NM_001287813.1(SNTG1):c.162+5660A>C	Lung cancer [RCV000107446]	uncertain significance	8	50408004	50408004	Human		name
8650385	CV126960	single nucleotide variant	NM_001287813.1(SNTG1):c.363+6560A>C	Lung cancer [RCV000107447]	uncertain significance	8	50457289	50457289	Human		name
8650386	CV126961	single nucleotide variant	NM_001287813.1(SNTG1):c.467-8916C>A	Lung cancer [RCV000107448]	uncertain significance	8	50521261	50521261	Human		name
8650387	CV126962	single nucleotide variant	NM_001287813.1(SNTG1):c.467-1231T>C	Lung cancer [RCV000107449]	uncertain significance	8	50528946	50528946	Human		name
8650375	CV126950	single nucleotide variant	NM_001287813.1(SNTG1):c.-103+8567C>G	Lung cancer [RCV000107437]	uncertain significance	8	49919611	49919611	Human		name
8650382	CV126957	single nucleotide variant	NM_001287813.1(SNTG1):c.-28+99678A>C	Lung cancer [RCV000107444]	uncertain significance	8	50272313	50272313	Human		name
8650383	CV126958	single nucleotide variant	NM_001287813.1(SNTG1):c.-27-83273G>A	Lung cancer [RCV000107445]	uncertain significance	8	50310939	50310939	Human		name
8650376	CV126951	single nucleotide variant	NM_001287813.1(SNTG1):c.-103+53680T>A	Lung cancer [RCV000107438]	uncertain significance	8	49964724	49964724	Human		name
8650377	CV126952	single nucleotide variant	NM_001287813.1(SNTG1):c.-103+76754G>A	Lung cancer [RCV000107439]	uncertain significance	8	49987798	49987798	Human		name
8650380	CV126955	single nucleotide variant	NM_001287813.1(SNTG1):c.-102-96604G>A	Lung cancer [RCV000107442]	uncertain significance	8	50075957	50075957	Human		name
8650381	CV126956	single nucleotide variant	NM_001287813.1(SNTG1):c.-102-36276T>A	Lung cancer [RCV000107443]	uncertain significance	8	50136285	50136285	Human		name
8650389	CV126964	single nucleotide variant	NM_001287813.1(SNTG1):c.1038+15911A>C	Lung cancer [RCV000107451]	uncertain significance	8	50674574	50674574	Human		name
8650378	CV126953	single nucleotide variant	NM_001287813.1(SNTG1):c.-102-122419G>A	Lung cancer [RCV000107440]	uncertain significance	8	50050142	50050142	Human		name
8650379	CV126954	single nucleotide variant	NM_001287813.1(SNTG1):c.-102-111896G>T	Lung cancer [RCV000107441]	uncertain significance	8	50060665	50060665	Human		name
401768851	CV2716756	single nucleotide variant	NM_018967.5(SNTG1):c.16G>A (p.Ala6Thr)	not specified [RCV004327798]	uncertain significance	8	50394254	50394254	Human		name
405291247	CV3215340	single nucleotide variant	NM_018967.5(SNTG1):c.186A>G (p.Arg62=)	SNTG1-related disorder [RCV003927410]	likely benign	8	50438566	50438566	Human		name , trait , alternate_id
156082249	CV2205423	single nucleotide variant	NM_018967.5(SNTG1):c.56A>C (p.Asp19Ala)	not specified [RCV004082368]	uncertain significance	8	50402238	50402238	Human		name
405286595	CV3192907	single nucleotide variant	NM_018967.5(SNTG1):c.927C>T (p.Ala309=)	SNTG1-related disorder [RCV003981615]	likely benign	8	50656986	50656986	Human		name , trait , alternate_id
405277172	CV3195355	single nucleotide variant	NM_018967.5(SNTG1):c.633A>G (p.Leu211=)	SNTG1-related disorder [RCV003904146]	benign	8	50536761	50536761	Human		name , trait , alternate_id
405269712	CV3201769	single nucleotide variant	NM_018967.5(SNTG1):c.432T>C (p.Ala144=)	SNTG1-related disorder [RCV003899675]	likely benign	8	50502846	50502846	Human		name , trait , alternate_id
405295433	CV3215952	single nucleotide variant	NM_018967.5(SNTG1):c.642G>C (p.Ser214=)	SNTG1-related disorder [RCV003937382]	likely benign	8	50536770	50536770	Human		name , trait , alternate_id
405278224	CV3216516	single nucleotide variant	NM_018967.5(SNTG1):c.309T>C (p.Asp103=)	SNTG1-related disorder [RCV003954438]	likely benign	8	50450587	50450587	Human		name , trait , alternate_id
405732027	CV3326337	single nucleotide variant	NM_018967.5(SNTG1):c.82C>T (p.Arg28Trp)	not specified [RCV004464461]	uncertain significance	8	50402264	50402264	Human		name
405732035	CV3326338	single nucleotide variant	NM_018967.5(SNTG1):c.83G>A (p.Arg28Gln)	not specified [RCV004464462]	uncertain significance	8	50402265	50402265	Human		name
617152687	CV4020924	single nucleotide variant	NM_018967.5(SNTG1):c.519C>T (p.Gly173=)	not provided [RCV005428677]	likely benign	8	50530229	50530229	Human		name
15157697	CV736702	single nucleotide variant	NM_018967.5(SNTG1):c.76A>C (p.Lys26Gln)	SNTG1-related disorder [RCV003912888]\|not provided [RCV000902581]	likely benign	8	50402258	50402258	Human		name , trait , alternate_id
329385118	CV2435264	single nucleotide variant	NM_018967.5(SNTG1):c.135T>G (p.Cys45Trp)	not specified [RCV004252897]	uncertain significance	8	50402317	50402317	Human		name
329354045	CV2436842	single nucleotide variant	NM_018967.5(SNTG1):c.278C>T (p.Ala93Val)	not specified [RCV004260237]	uncertain significance	8	50450556	50450556	Human		name
405278622	CV3216754	single nucleotide variant	NM_018967.5(SNTG1):c.250G>A (p.Val84Ile)	SNTG1-related disorder [RCV003954632]	likely benign	8	50449698	50449698	Human		name , trait , alternate_id
407503750	CV3474679	single nucleotide variant	NM_018967.5(SNTG1):c.245T>G (p.Val82Gly)	not specified [RCV004670357]	uncertain significance	8	50449693	50449693	Human		name
597740926	CV3607187	single nucleotide variant	NM_018967.5(SNTG1):c.170C>T (p.Thr57Met)	not specified [RCV004864756]	uncertain significance	8	50438550	50438550	Human		name
598171609	CV3911634	single nucleotide variant	NM_018967.5(SNTG1):c.286T>G (p.Ser96Ala)	not specified [RCV005284871]	uncertain significance	8	50450564	50450564	Human		name
15168396	CV723135	single nucleotide variant	NM_018967.5(SNTG1):c.1134C>T (p.Leu378=)	not provided [RCV000883055]	benign\|likely benign	8	50704695	50704695	Human		name
156041027	CV2310857	single nucleotide variant	NM_018967.5(SNTG1):c.523C>T (p.His175Tyr)	not specified [RCV004163901]	uncertain significance	8	50530233	50530233	Human		name
329370035	CV2424914	single nucleotide variant	NM_018967.5(SNTG1):c.422G>C (p.Arg141Thr)	not provided [RCV003491341]\|not specified [RCV004248791]	uncertain significance	8	50502836	50502836	Human		name
401773784	CV2691406	single nucleotide variant	NM_018967.5(SNTG1):c.545A>G (p.Asn182Ser)	not specified [RCV004305268]	uncertain significance	8	50530255	50530255	Human		name
401729016	CV2693992	single nucleotide variant	NM_018967.5(SNTG1):c.403A>G (p.Thr135Ala)	not specified [RCV004300279]	uncertain significance	8	50502817	50502817	Human		name
401759088	CV2712406	single nucleotide variant	NM_018967.5(SNTG1):c.799A>G (p.Thr267Ala)	not specified [RCV004313879]	uncertain significance	8	50553168	50553168	Human		name
401729451	CV2733065	single nucleotide variant	NM_018967.5(SNTG1):c.385G>A (p.Gly129Arg)	not specified [RCV004331999]	uncertain significance	8	50502799	50502799	Human		name
401857722	CV2777736	single nucleotide variant	NM_018967.5(SNTG1):c.857A>G (p.Tyr286Cys)	not specified [RCV004345571]	uncertain significance	8	50656916	50656916	Human		name
405286083	CV3192034	single nucleotide variant	NM_018967.5(SNTG1):c.664G>A (p.Gly222Ser)	SNTG1-related disorder [RCV003923961]	likely benign	8	50536792	50536792	Human		name , trait , alternate_id
405266763	CV3202085	single nucleotide variant	NM_018967.5(SNTG1):c.722C>G (p.Thr241Ser)	SNTG1-related disorder [RCV003911565]	benign	8	50553091	50553091	Human		name , trait , alternate_id
405278574	CV3220327	single nucleotide variant	NM_018967.5(SNTG1):c.361G>C (p.Val121Leu)	SNTG1-related disorder [RCV003976558]	likely benign	8	50450727	50450727	Human		name , trait , alternate_id
405731975	CV3326330	single nucleotide variant	NM_018967.5(SNTG1):c.301A>G (p.Ile101Val)	not specified [RCV004464454]	uncertain significance	8	50450579	50450579	Human		name
405731983	CV3326331	single nucleotide variant	NM_018967.5(SNTG1):c.322A>T (p.Ile108Leu)	not specified [RCV004464455]	uncertain significance	8	50450688	50450688	Human		name
405731989	CV3326332	single nucleotide variant	NM_018967.5(SNTG1):c.493A>G (p.Thr165Ala)	not specified [RCV004464456]	uncertain significance	8	50530203	50530203	Human		name
405731995	CV3326333	single nucleotide variant	NM_018967.5(SNTG1):c.548C>G (p.Thr183Arg)	not specified [RCV004464457]	uncertain significance	8	50530258	50530258	Human		name
405732003	CV3326334	single nucleotide variant	NM_018967.5(SNTG1):c.640T>G (p.Ser214Ala)	not specified [RCV004464458]	uncertain significance	8	50536768	50536768	Human		name
405732011	CV3326335	single nucleotide variant	NM_018967.5(SNTG1):c.697G>T (p.Val233Phe)	not specified [RCV004464459]	uncertain significance	8	50553066	50553066	Human		name
405732020	CV3326336	single nucleotide variant	NM_018967.5(SNTG1):c.804G>C (p.Lys268Asn)	not specified [RCV004464460]	uncertain significance	8	50553173	50553173	Human		name
407503736	CV3474675	single nucleotide variant	NM_018967.5(SNTG1):c.757G>A (p.Val253Ile)	not specified [RCV004670353]	likely benign	8	50553126	50553126	Human		name
407503743	CV3474677	single nucleotide variant	NM_018967.5(SNTG1):c.889C>A (p.Pro297Thr)	not specified [RCV004670355]	uncertain significance	8	50656948	50656948	Human		name
407503746	CV3474678	single nucleotide variant	NM_018967.5(SNTG1):c.529A>T (p.Asn177Tyr)	not specified [RCV004670356]	uncertain significance	8	50530239	50530239	Human		name
407525297	CV3474680	single nucleotide variant	NM_018967.5(SNTG1):c.877C>G (p.Arg293Gly)	not specified [RCV004679119]	uncertain significance	8	50656936	50656936	Human		name
407525298	CV3474681	single nucleotide variant	NM_018967.5(SNTG1):c.572G>T (p.Trp191Leu)	not specified [RCV004679120]	uncertain significance	8	50536700	50536700	Human		name
597745086	CV3607184	single nucleotide variant	NM_018967.5(SNTG1):c.703G>T (p.Ala235Ser)	not specified [RCV004865600]	uncertain significance	8	50553072	50553072	Human		name
597745096	CV3607186	single nucleotide variant	NM_018967.5(SNTG1):c.784A>T (p.Asn262Tyr)	not specified [RCV004865602]	uncertain significance	8	50553153	50553153	Human		name
598171594	CV3911631	single nucleotide variant	NM_018967.5(SNTG1):c.752A>G (p.Asp251Gly)	not specified [RCV005284868]	uncertain significance	8	50553121	50553121	Human		name
598171604	CV3911633	single nucleotide variant	NM_018967.5(SNTG1):c.377G>A (p.Arg126Gln)	not specified [RCV005284870]	uncertain significance	8	50502791	50502791	Human		name
156122287	CV2276083	single nucleotide variant	NM_018967.5(SNTG1):c.1262T>C (p.Ile421Thr)	not specified [RCV004141752]	uncertain significance	8	50708956	50708956	Human		name
329371956	CV2442959	single nucleotide variant	NM_018967.5(SNTG1):c.1042A>G (p.Ser348Gly)	not specified [RCV004253554]	uncertain significance	8	50704603	50704603	Human		name
401762304	CV2696078	single nucleotide variant	NM_018967.5(SNTG1):c.1240A>G (p.Ile414Val)	not specified [RCV004310143]	uncertain significance	8	50708934	50708934	Human		name
405731968	CV3326329	single nucleotide variant	NM_018967.5(SNTG1):c.1538C>T (p.Ala513Val)	not specified [RCV004464453]	uncertain significance	8	50792813	50792813	Human		name
597745080	CV3607183	single nucleotide variant	NM_018967.5(SNTG1):c.1144G>C (p.Glu382Gln)	not specified [RCV004865599]	uncertain significance	8	50704705	50704705	Human		name
597745091	CV3607185	single nucleotide variant	NM_018967.5(SNTG1):c.1238C>A (p.Thr413Lys)	not specified [RCV004865601]	uncertain significance	8	50708932	50708932	Human		name
598171587	CV3911630	single nucleotide variant	NM_018967.5(SNTG1):c.1368T>A (p.Asn456Lys)	not specified [RCV005284867]	uncertain significance	8	50752084	50752084	Human		name
598171599	CV3911632	single nucleotide variant	NM_018967.5(SNTG1):c.1226T>C (p.Leu409Pro)	not specified [RCV005284869]	uncertain significance	8	50708920	50708920	Human		name
9831807	CV166976	deletion	NM_018967.5(SNTG1):c.-27-79544_-27-75960del	Gestational diabetes mellitus uncontrolled [RCV000161542]	not provided	8	50314668	50318252	Human		name

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