Sap30l 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)

14 records found for search term Sap30l

Refine Term:

Assembly:

Chr

Sort By:

Export

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156375554	CV2210227	single nucleotide variant	NM_024632.6(SAP30L):c.56C>T (p.Ala19Val)	not specified [RCV004087604]	uncertain significance	5	154446660	154446660	Human		name
156344692	CV2381878	single nucleotide variant	NM_024632.6(SAP30L):c.36A>C (p.Glu12Asp)	not specified [RCV004225822]	uncertain significance	5	154446640	154446640	Human		name
155934056	CV2399440	single nucleotide variant	NM_024632.6(SAP30L):c.40C>A (p.Pro14Thr)	not specified [RCV004242715]	uncertain significance	5	154446644	154446644	Human		name
597789833	CV3605002	single nucleotide variant	NM_024632.6(SAP30L):c.52C>T (p.Pro18Ser)	not specified [RCV004855855]	uncertain significance	5	154446656	154446656	Human		name
156130694	CV2210084	single nucleotide variant	NM_024632.6(SAP30L):c.277A>G (p.Ser93Gly)	not specified [RCV004078560]	uncertain significance	5	154451166	154451166	Human		name
155917938	CV2236691	single nucleotide variant	NM_024632.6(SAP30L):c.100G>A (p.Asp34Asn)	not specified [RCV004110647]	uncertain significance	5	154446704	154446704	Human		name
407460496	CV3483619	single nucleotide variant	NM_024632.6(SAP30L):c.136T>G (p.Ser46Ala)	not specified [RCV004658468]	uncertain significance	5	154446740	154446740	Human		name
156352247	CV2323934	single nucleotide variant	NM_024632.6(SAP30L):c.484A>G (p.Ile162Val)	not specified [RCV004176460]	uncertain significance	5	154455960	154455960	Human		name
156165843	CV2373536	single nucleotide variant	NM_024632.6(SAP30L):c.319C>A (p.Pro107Thr)	not specified [RCV004222642]	uncertain significance	5	154451208	154451208	Human		name
329394504	CV2469906	single nucleotide variant	NM_024632.6(SAP30L):c.379A>C (p.Lys127Gln)	not specified [RCV004285373]	uncertain significance	5	154453456	154453456	Human		name
401731811	CV2712167	single nucleotide variant	NM_024632.6(SAP30L):c.319C>G (p.Pro107Ala)	not specified [RCV004311887]	uncertain significance	5	154451208	154451208	Human		name
401885896	CV2774885	single nucleotide variant	NM_024632.6(SAP30L):c.527C>T (p.Ser176Leu)	not specified [RCV004343964]	uncertain significance	5	154456003	154456003	Human		name
597789825	CV3605000	single nucleotide variant	NM_024632.6(SAP30L):c.499A>G (p.Ser167Gly)	not specified [RCV004855853]	uncertain significance	5	154455975	154455975	Human		name
597789829	CV3605001	single nucleotide variant	NM_024632.6(SAP30L):c.316A>G (p.Ile106Val)	not specified [RCV004855854]	uncertain significance	5	154451205	154451205	Human		name