Product Details

SNP ID
rs113568283
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:1387370 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTATTTTCCCGGATTATCCGCCCGC[C/T]CCCGTGACCTGCTTCGAGAACGGGA
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 1340 Intron NP_001034666.1
NM_001320153.1 1340 Missense Mutation GAG,GGG E253G NP_001307082.1
NM_001320155.1 1340 Missense Mutation GAG,GGG E253G NP_001307084.1
NM_030937.4 1340 Missense Mutation GAG,GGG E475G NP_112199.2
XM_011542216.2 1340 Missense Mutation GAG,GGG E508G XP_011540518.1
XM_011542219.2 1340 Missense Mutation GAG,GGG E344G XP_011540521.1
XM_011542221.2 1340 Missense Mutation GAG,GGG E253G XP_011540523.1
XM_017002420.1 1340 Missense Mutation GAG,GGG E353G XP_016857909.1
XM_017002421.1 1340 Missense Mutation GAG,GGG E344G XP_016857910.1
XM_017002422.1 1340 Missense Mutation GAG,GGG E253G XP_016857911.1
XM_017002423.1 1340 Intron XP_016857912.1

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