Product Details

SNP ID
rs200296263
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:38879191 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTCCCTCTCTGTTGTCCTGGCCTC[A/G]TCCTTGGCAGGTGGCGGGGACTTCT
Phenotype
MIM: 604480
Polymorphism
A/G, 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 1321 Intron NP_001182762.1
NM_198445.3 1321 Intron NP_940847.1
XM_006723015.2 1321 Intron XP_006723078.1
XM_006723016.2 1321 Intron XP_006723079.1
XM_011526454.2 1321 Intron XP_011524756.1
XM_011526455.2 1321 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 1321 UTR 3 NP_001180215.1
NM_012237.3 1321 Silent Mutation GAC,GAT D378D NP_036369.2
NM_030593.2 1321 Silent Mutation GAC,GAT D341D NP_085096.1
XM_006723111.1 1321 Silent Mutation GAC,GAT D341D XP_006723174.1
XM_011526654.1 1321 Silent Mutation GAC,GAT D341D XP_011524956.1
XM_011526655.1 1321 Silent Mutation GAC,GAT D308D XP_011524957.1
XM_017026500.1 1321 Silent Mutation GAC,GAT D255D XP_016881989.1

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