Product Details

SNP ID
rs112675079
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:1387780 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGTGCGCCCTGAGGCACACACCTC[C/T]TCTTAGGAGACGCTGATCGGGATGG
Phenotype
MIM: 613482
Polymorphism
C/T, 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 1124 Intron NP_001034666.1
NM_001320153.1 1124 Missense Mutation NP_001307082.1
NM_001320155.1 1124 Missense Mutation NP_001307084.1
NM_030937.4 1124 Missense Mutation NP_112199.2
XM_011542216.2 1124 Missense Mutation XP_011540518.1
XM_011542219.2 1124 Missense Mutation XP_011540521.1
XM_011542221.2 1124 Missense Mutation XP_011540523.1
XM_017002420.1 1124 Missense Mutation XP_016857909.1
XM_017002421.1 1124 Missense Mutation XP_016857910.1
XM_017002422.1 1124 Missense Mutation XP_016857911.1
XM_017002423.1 1124 Intron XP_016857912.1

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