Product Details

SNP ID
rs151205333
Assay Type
Functionally Tested
NCBI dbSNP Submissions
6
Location
Chr.1:1387489 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAATCTCAGAGCCTTTGTAGGGAGC[A/G]CTGCGGGGGGCCTGTCTCGGTGGGG
Phenotype
MIM: 613482
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CCNL2 PubMed Links

Gene Details

Gene
CCNL2
Gene Name
cyclin L2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039577.3 1221 Intron NP_001034666.1
NM_001320153.1 1221 Silent Mutation AGC,AGT S213S NP_001307082.1
NM_001320155.1 1221 Silent Mutation AGC,AGT S213S NP_001307084.1
NM_030937.4 1221 Silent Mutation AGC,AGT S435S NP_112199.2
XM_011542216.2 1221 Silent Mutation AGC,AGT S468S XP_011540518.1
XM_011542219.2 1221 Silent Mutation AGC,AGT S304S XP_011540521.1
XM_011542221.2 1221 Silent Mutation AGC,AGT S213S XP_011540523.1
XM_017002420.1 1221 Silent Mutation AGC,AGT S313S XP_016857909.1
XM_017002421.1 1221 Silent Mutation AGC,AGT S304S XP_016857910.1
XM_017002422.1 1221 Silent Mutation AGC,AGT S213S XP_016857911.1
XM_017002423.1 1221 Intron XP_016857912.1

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