Rbbp7 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)

18 records found for search term Rbbp7

Refine Term:

Sort By:

Export

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401931097	CV2823943	single nucleotide variant	NM_002893.4(RBBP7):c.17-341A>C	not provided [RCV003441061]	likely benign	X	16869561	16869561	Human		name
401931099	CV2823944	single nucleotide variant	NM_002893.4(RBBP7):c.17-374G>T	not provided [RCV003441062]	likely benign	X	16869594	16869594	Human		name
407507281	CV3468784	single nucleotide variant	NM_002893.4(RBBP7):c.16+401C>T	not specified [RCV004671668]	uncertain significance	X	16869637	16869637	Human		name
598186129	CV3902440	single nucleotide variant	NM_002893.4(RBBP7):c.17-286C>T	not specified [RCV005266032]	uncertain significance	X	16869506	16869506	Human		name
598186138	CV3902441	single nucleotide variant	NM_002893.4(RBBP7):c.17-294C>T	not specified [RCV005266033]	uncertain significance	X	16869514	16869514	Human		name
15195830	CV729523	single nucleotide variant	NM_002893.4(RBBP7):c.66C>A (p.Ile22=)	not provided [RCV000889613]	benign	X	16869171	16869171	Human		name
401931096	CV2823942	single nucleotide variant	NM_002893.4(RBBP7):c.46A>G (p.Ile16Val)	not provided [RCV003441060]	uncertain significance	X	16869191	16869191	Human		name
156225822	CV2400983	single nucleotide variant	NM_002893.4(RBBP7):c.260A>G (p.Asn87Ser)	not specified [RCV004244267]	uncertain significance	X	16863002	16863002	Human		name
156235616	CV2267998	single nucleotide variant	NM_002893.4(RBBP7):c.814A>G (p.Thr272Ala)	not specified [RCV004136556]	uncertain significance	X	16852820	16852820	Human		name
407467466	CV3468783	single nucleotide variant	NM_002893.4(RBBP7):c.799T>G (p.Leu267Val)	not specified [RCV004660728]	uncertain significance	X	16852835	16852835	Human		name
597784657	CV3589616	single nucleotide variant	NM_002893.4(RBBP7):c.907C>T (p.Arg303Cys)	not specified [RCV004854531]	uncertain significance	X	16852607	16852607	Human		name
597707888	CV3589617	single nucleotide variant	NM_002893.4(RBBP7):c.304G>A (p.Gly102Ser)	not specified [RCV004860663]	uncertain significance	X	16862958	16862958	Human		name
597784660	CV3589618	single nucleotide variant	NM_002893.4(RBBP7):c.776A>G (p.Asn259Ser)	not specified [RCV004854532]	uncertain significance	X	16852858	16852858	Human		name
597730022	CV3703346	duplication	NM_002893.4(RBBP7):c.1200dup (p.Trp401fs)	Spermatogenic failure, X-linked, 9 [RCV004995667]	pathogenic	X	16845836	16845837	Human	1	name
598186148	CV3902442	single nucleotide variant	NM_002893.4(RBBP7):c.851G>T (p.Ser284Ile)	not specified [RCV005266034]	uncertain significance	X	16852783	16852783	Human		name
155901307	CV2294416	single nucleotide variant	NM_002893.4(RBBP7):c.1263G>C (p.Glu421Asp)	not specified [RCV004159926]	uncertain significance	X	16845050	16845050	Human		name
405669696	CV3308722	single nucleotide variant	NM_002893.4(RBBP7):c.1242T>A (p.Asp414Glu)	not specified [RCV004441003]	uncertain significance	X	16845071	16845071	Human		name
597784653	CV3589614	single nucleotide variant	NM_002893.4(RBBP7):c.1151A>G (p.Asn384Ser)	not specified [RCV004854530]	uncertain significance	X	16845886	16845886	Human		name