Nr1h2 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)

13 records found for search term Nr1h2

Refine Term:

Assembly:

Chr

Sort By:

Export

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150453943	CV1265927	single nucleotide variant	NM_007121.7(NR1H2):c.182-80T>C	not provided [RCV001692504]	benign	19	50378069	50378069	Human		name
598264448	CV3997933	single nucleotide variant	NM_007121.7(NR1H2):c.23C>A (p.Ser8Tyr)	not specified [RCV005387756]	uncertain significance	19	50377628	50377628	Human		name
156337311	CV2267245	single nucleotide variant	NM_007121.7(NR1H2):c.50G>A (p.Gly17Asp)	not specified [RCV004133925]	uncertain significance	19	50377739	50377739	Human		name
405693767	CV3362476	single nucleotide variant	NM_007121.7(NR1H2):c.77C>T (p.Ser26Phe)	not specified [RCV004491224]	uncertain significance	19	50377766	50377766	Human		name
407476735	CV3465769	single nucleotide variant	NM_007121.7(NR1H2):c.71C>T (p.Pro24Leu)	not specified [RCV004638658]	uncertain significance	19	50377760	50377760	Human		name
597687274	CV3566667	single nucleotide variant	NM_007121.7(NR1H2):c.55C>T (p.Pro19Ser)	not specified [RCV004838198]	uncertain significance	19	50377744	50377744	Human		name
597687263	CV3566668	single nucleotide variant	NM_007121.7(NR1H2):c.34C>T (p.Pro12Ser)	not specified [RCV004838199]	uncertain significance	19	50377639	50377639	Human		name
598264442	CV3997932	single nucleotide variant	NM_007121.7(NR1H2):c.64G>A (p.Gly22Ser)	not specified [RCV005387755]	likely benign	19	50377753	50377753	Human		name
401742539	CV2697802	single nucleotide variant	NM_007121.7(NR1H2):c.212G>T (p.Arg71Leu)	not specified [RCV004300522]	uncertain significance	19	50378179	50378179	Human		name
405693761	CV3362475	single nucleotide variant	NM_007121.7(NR1H2):c.113G>T (p.Trp38Leu)	not specified [RCV004491223]	uncertain significance	19	50377802	50377802	Human		name
407516686	CV3465768	single nucleotide variant	NM_007121.7(NR1H2):c.121G>T (p.Gly41Cys)	not specified [RCV004650365]	uncertain significance	19	50377810	50377810	Human		name
597687283	CV3566666	single nucleotide variant	NM_007121.7(NR1H2):c.119G>A (p.Gly40Glu)	not specified [RCV004838197]	uncertain significance	19	50377808	50377808	Human		name
13827371	CV578572	single nucleotide variant	NM_007121.7(NR1H2):c.950G>A (p.Arg317Lys)	not provided [RCV000714775]	uncertain significance	19	50379802	50379802	Human		name