Praf2 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 All species
(View Results for all Objects and Ontologies)

14 records found for search term Praf2

Refine Term:

Sort By:

Export

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597770591	CV3584277	single nucleotide variant	NM_007213.3(PRAF2):c.5C>T (p.Ser2Leu)	not specified [RCV004851153]	uncertain significance	X	49073983	49073983	Human		name
156207186	CV2298024	single nucleotide variant	NM_007213.3(PRAF2):c.59C>G (p.Ala20Gly)	not specified [RCV004157924]	uncertain significance	X	49073929	49073929	Human		name
405653488	CV3378761	single nucleotide variant	NM_007213.3(PRAF2):c.95G>T (p.Arg32Leu)	not specified [RCV004510304]	uncertain significance	X	49073893	49073893	Human		name
156102726	CV2260448	single nucleotide variant	NM_007213.3(PRAF2):c.137C>G (p.Thr46Ser)	not specified [RCV004123243]	uncertain significance	X	49073851	49073851	Human		name
156259277	CV2304940	single nucleotide variant	NM_007213.3(PRAF2):c.151T>C (p.Cys51Arg)	not specified [RCV004168844]	uncertain significance	X	49073837	49073837	Human		name
329386082	CV2458811	single nucleotide variant	NM_007213.3(PRAF2):c.106C>G (p.Arg36Gly)	not specified [RCV004270235]	uncertain significance	X	49073882	49073882	Human		name
597770582	CV3584275	single nucleotide variant	NM_007213.3(PRAF2):c.184G>A (p.Val62Met)	not specified [RCV004851151]	uncertain significance	X	49072646	49072646	Human		name
156385235	CV2227859	single nucleotide variant	NM_007213.3(PRAF2):c.376A>G (p.Ser126Gly)	not specified [RCV004094498]	uncertain significance	X	49072454	49072454	Human		name
156138915	CV2236799	single nucleotide variant	NM_007213.3(PRAF2):c.386G>A (p.Gly129Glu)	not specified [RCV004112565]	uncertain significance	X	49072444	49072444	Human		name
401762317	CV2723397	single nucleotide variant	NM_007213.3(PRAF2):c.416C>T (p.Ser139Leu)	not specified [RCV004329603]	uncertain significance	X	49071990	49071990	Human		name
401894831	CV2785358	single nucleotide variant	NM_007213.3(PRAF2):c.313G>A (p.Ala105Thr)	not specified [RCV004357107]	uncertain significance	X	49072517	49072517	Human		name
405653485	CV3378759	single nucleotide variant	NM_007213.3(PRAF2):c.365C>G (p.Thr122Ser)	not specified [RCV004510302]	uncertain significance	X	49072465	49072465	Human		name
405653487	CV3378760	single nucleotide variant	NM_007213.3(PRAF2):c.406G>T (p.Val136Leu)	not specified [RCV004510303]	uncertain significance	X	49072000	49072000	Human		name
407464828	CV3467926	single nucleotide variant	NM_007213.3(PRAF2):c.443A>G (p.Lys148Arg)	not specified [RCV004660048]	uncertain significance	X	49071963	49071963	Human		name