Product Details

SNP ID
rs139865828
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:1387393 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTCCCGTGACCTGCTTCGAGAACG[A/G]GAAGAACTCCGGCTCCGAGACTTGT
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 1317 Intron NP_001034666.1
NM_001320153.1 1317 Silent Mutation TCC,TCT S245S NP_001307082.1
NM_001320155.1 1317 Silent Mutation TCC,TCT S245S NP_001307084.1
NM_030937.4 1317 Silent Mutation TCC,TCT S467S NP_112199.2
XM_011542216.2 1317 Silent Mutation TCC,TCT S500S XP_011540518.1
XM_011542219.2 1317 Silent Mutation TCC,TCT S336S XP_011540521.1
XM_011542221.2 1317 Silent Mutation TCC,TCT S245S XP_011540523.1
XM_017002420.1 1317 Silent Mutation TCC,TCT S345S XP_016857909.1
XM_017002421.1 1317 Silent Mutation TCC,TCT S336S XP_016857910.1
XM_017002422.1 1317 Silent Mutation TCC,TCT S245S XP_016857911.1
XM_017002423.1 1317 Intron XP_016857912.1

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