Product Details

SNP ID
rs199521745
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:38879206 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTGGCCTCGTCCTTGGCAGGTGG[C/T]GGGGACTTCTTGGGGGAAGCTGAAG
Phenotype
MIM: 604480
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RINL PubMed Links

Gene Details

Gene
RINL
Gene Name
Ras and Rab interactor like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001195833.1 1306 Intron NP_001182762.1
NM_198445.3 1306 Intron NP_940847.1
XM_006723015.2 1306 Intron XP_006723078.1
XM_006723016.2 1306 Intron XP_006723079.1
XM_011526454.2 1306 Intron XP_011524756.1
XM_011526455.2 1306 Intron XP_011524757.1
Gene
SIRT2
Gene Name
sirtuin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001193286.1 1306 UTR 3 NP_001180215.1
NM_012237.3 1306 Silent Mutation CCA,CCG P373P NP_036369.2
NM_030593.2 1306 Silent Mutation CCA,CCG P336P NP_085096.1
XM_006723111.1 1306 Silent Mutation CCA,CCG P336P XP_006723174.1
XM_011526654.1 1306 Silent Mutation CCA,CCG P336P XP_011524956.1
XM_011526655.1 1306 Silent Mutation CCA,CCG P303P XP_011524957.1
XM_017026500.1 1306 Silent Mutation CCA,CCG P250P XP_016881989.1

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