Gpsm3 Variant Search Result - Rat Genome Database

Submit Data | Help | Video Tutorials | News | Publications | Download | REST API | Citing RGD | Contact

Advanced Search (OLGA)

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

17 records found for search term Gpsm3

Refine Term:

Assembly:

Chr

Sort By:

Export

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150508732	CV1284355	single nucleotide variant	NM_022107.3(GPSM3):c.-102+235C>T	not provided [RCV001720463]	benign	6	32194075	32194075	Human	6	name
156395336	CV2329135	single nucleotide variant	NM_001276501.2(GPSM3):c.41A>C (p.Gln14Pro)	not specified [RCV004173896]	uncertain significance	6	32192473	32192473	Human		name
401762063	CV2713997	single nucleotide variant	NM_001276501.2(GPSM3):c.49C>T (p.Pro17Ser)	not specified [RCV004315407]	likely benign	6	32192244	32192244	Human		name
405756117	CV3252325	single nucleotide variant	NM_001276501.2(GPSM3):c.71C>T (p.Pro24Leu)	not specified [RCV004393481]	uncertain significance	6	32192222	32192222	Human		name
597770122	CV3681826	single nucleotide variant	NM_001276501.2(GPSM3):c.49C>G (p.Pro17Ala)	not specified [RCV004928240]	uncertain significance	6	32192244	32192244	Human		name
15169684	CV699535	single nucleotide variant	NM_001276501.2(GPSM3):c.435G>A (p.Gly145=)	not provided [RCV000949506]	benign	6	32191414	32191414	Human		name
155971994	CV2228006	single nucleotide variant	NM_001276501.2(GPSM3):c.212A>G (p.Glu71Gly)	not specified [RCV004096250]	uncertain significance	6	32191842	32191842	Human		name
155949857	CV2267730	single nucleotide variant	NM_001276501.2(GPSM3):c.125C>T (p.Pro42Leu)	not specified [RCV004134264]	uncertain significance	6	32192168	32192168	Human		name
401771722	CV2693472	single nucleotide variant	NM_001276501.2(GPSM3):c.221C>T (p.Ser74Phe)	not specified [RCV004295418]	uncertain significance	6	32191833	32191833	Human		name
401872256	CV2793051	single nucleotide variant	NM_001276501.2(GPSM3):c.137G>A (p.Arg46His)	not specified [RCV004360381]	likely benign	6	32192156	32192156	Human		name
405756096	CV3252322	single nucleotide variant	NM_001276501.2(GPSM3):c.136C>T (p.Arg46Cys)	not specified [RCV004393478]	uncertain significance	6	32192157	32192157	Human		name
405756101	CV3252323	single nucleotide variant	NM_001276501.2(GPSM3):c.226C>T (p.Arg76Cys)	not specified [RCV004393479]	uncertain significance	6	32191828	32191828	Human		name
597745933	CV3681824	single nucleotide variant	NM_001276501.2(GPSM3):c.224G>A (p.Arg75His)	not specified [RCV004922593]	uncertain significance	6	32191830	32191830	Human		name
597745937	CV3681825	single nucleotide variant	NM_001276501.2(GPSM3):c.219G>C (p.Gln73His)	not specified [RCV004922594]	uncertain significance	6	32191835	32191835	Human		name
597770127	CV3681827	single nucleotide variant	NM_001276501.2(GPSM3):c.227G>A (p.Arg76His)	not specified [RCV004928241]	uncertain significance	6	32191827	32191827	Human		name
15183701	CV699536	single nucleotide variant	NM_001276501.2(GPSM3):c.139C>G (p.His47Asp)	not provided [RCV000952526]	benign	6	32192154	32192154	Human		name
405756108	CV3252324	single nucleotide variant	NM_001276501.2(GPSM3):c.412T>G (p.Leu138Val)	not specified [RCV004393480]	uncertain significance	6	32191437	32191437	Human		name