Igsf9b 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)

11 records found for search term Igsf9b

Refine Term:

Sort By:

Export

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405800208	CV3274717	single nucleotide variant	NM_001277285.4(IGSF9B):c.822C>T (p.Asn274=)	not specified [RCV004402855]	likely benign	11	133935762	133935762	Human		name
401929351	CV2810030	single nucleotide variant	NM_001277285.4(IGSF9B):c.2454G>A (p.Ser818=)	not provided [RCV003390141]	likely benign	11	133921271	133921271	Human		name
598270002	CV3975946	single nucleotide variant	NM_001277285.4(IGSF9B):c.2805C>T (p.Arg935=)	not specified [RCV005350014]	likely benign	11	133920920	133920920	Human		name
15171881	CV706385	single nucleotide variant	NM_001277285.4(IGSF9B):c.2637C>T (p.Phe879=)	not provided [RCV000947403]	benign	11	133921088	133921088	Human		name
15168434	CV729776	single nucleotide variant	NM_001277285.4(IGSF9B):c.1260C>A (p.Pro420=)	not provided [RCV000879817]	benign\|likely benign	11	133931561	133931561	Human		name
401929354	CV2810029	single nucleotide variant	NM_001277285.4(IGSF9B):c.3232C>A (p.Arg1078=)	not provided [RCV003390140]	likely benign	11	133920493	133920493	Human		name
15171165	CV774296	single nucleotide variant	NM_001277285.4(IGSF9B):c.3477C>T (p.Gly1159=)	not provided [RCV000938138]	likely benign	11	133920248	133920248	Human		name
8633944	CV89160	single nucleotide variant	NM_001277285.1(IGSF9B):c.2660C>T (p.Pro887Leu)	Malignant melanoma [RCV000069257]	not provided	11	133921065	133921065	Human		name
408367853	CV3517643	single nucleotide variant	NM_001277285.4(IGSF9B):c.3542C>T (p.Pro1181Leu)	IGSF9B-related condition [RCV004759271]	uncertain significance	11	133920183	133920183	Human		name , trait
15171876	CV706386	single nucleotide variant	NM_001277285.4(IGSF9B):c.3545G>A (p.Arg1182Gln)	not provided [RCV000947402]	likely benign	11	133920180	133920180	Human		name
15171870	CV706387	single nucleotide variant	NM_001277285.4(IGSF9B):c.3835G>A (p.Ala1279Thr)	not provided [RCV000947401]	benign	11	133919890	133919890	Human		name