Nrg4 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 Nrg4

Refine Term:

Sort By:

Export

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8584570	CV119144	single nucleotide variant	NM_138573.3(NRG4):c.105-15566G>A	Lung cancer [RCV000099664]	uncertain significance	15	75977540	75977540	Human		name
155984264	CV2367895	single nucleotide variant	NM_138573.4(NRG4):c.68G>T (p.Cys23Phe)	not specified [RCV004222996]	uncertain significance	15	76009236	76009236	Human		name
401777387	CV2707933	single nucleotide variant	NM_138573.4(NRG4):c.89C>T (p.Pro30Leu)	not specified [RCV004309198]	uncertain significance	15	76009215	76009215	Human		name
597706459	CV3576823	single nucleotide variant	NM_138573.4(NRG4):c.71A>T (p.Tyr24Phe)	not specified [RCV004840346]	uncertain significance	15	76009233	76009233	Human		name
155934193	CV2229103	single nucleotide variant	NM_138573.4(NRG4):c.134G>T (p.Cys45Phe)	not specified [RCV004098872]	uncertain significance	15	75961945	75961945	Human		name
156086814	CV2336807	single nucleotide variant	NM_138573.4(NRG4):c.167A>C (p.Gln56Pro)	not specified [RCV004190428]	uncertain significance	15	75961912	75961912	Human		name
405708791	CV3362719	single nucleotide variant	NM_138573.4(NRG4):c.233C>A (p.Ala78Asp)	not specified [RCV004493534]	uncertain significance	15	75961846	75961846	Human		name
405708799	CV3362720	single nucleotide variant	NM_138573.4(NRG4):c.269G>C (p.Arg90Thr)	not specified [RCV004493535]	uncertain significance	15	75955994	75955994	Human		name
407516885	CV3465883	single nucleotide variant	NM_138573.4(NRG4):c.122C>T (p.Thr41Ile)	not specified [RCV004650438]	uncertain significance	15	75961957	75961957	Human		name
407516889	CV3465885	single nucleotide variant	NM_138573.4(NRG4):c.289G>A (p.Asp97Asn)	not specified [RCV004650440]	uncertain significance	15	75955974	75955974	Human		name
597706473	CV3576824	single nucleotide variant	NM_138573.4(NRG4):c.276T>G (p.Ser92Arg)	not specified [RCV004840347]	uncertain significance	15	75955987	75955987	Human		name
15135538	CV714617	single nucleotide variant	NM_138573.4(NRG4):c.109G>A (p.Val37Ile)	not provided [RCV000965305]	benign	15	75961970	75961970	Human		name
401896218	CV2773842	single nucleotide variant	NM_138573.4(NRG4):c.310A>G (p.Ser104Gly)	not specified [RCV004358285]	uncertain significance	15	75955953	75955953	Human		name
405708806	CV3362721	single nucleotide variant	NM_138573.4(NRG4):c.308C>T (p.Thr103Met)	not specified [RCV004493536]	uncertain significance	15	75955955	75955955	Human		name