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ATGACTTTTCTTCTTGTATTTTCCC[A/G]GATTATCCGCCCGCTCCCGTGACCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
14 submissions
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Phenotype: |
MIM: 613482 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCNL2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CCNL2 - cyclin L2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039577.3 | 1355 | Intron | NP_001034666.1 | |||
NM_001320153.1 | 1355 | Missense Mutation | CCG,CTG | P,L 258 | NP_001307082.1 | |
NM_001320155.1 | 1355 | Missense Mutation | CCG,CTG | P,L 258 | NP_001307084.1 | |
NM_030937.4 | 1355 | Missense Mutation | CCG,CTG | P,L 480 | NP_112199.2 | |
XM_011542216.2 | 1355 | Missense Mutation | CCG,CTG | P,L 513 | XP_011540518.1 | |
XM_011542219.2 | 1355 | Missense Mutation | CCG,CTG | P,L 349 | XP_011540521.1 | |
XM_011542221.2 | 1355 | Missense Mutation | CCG,CTG | P,L 258 | XP_011540523.1 | |
XM_017002420.1 | 1355 | Missense Mutation | CCG,CTG | P,L 358 | XP_016857909.1 | |
XM_017002421.1 | 1355 | Missense Mutation | CCG,CTG | P,L 349 | XP_016857910.1 | |
XM_017002422.1 | 1355 | Missense Mutation | CCG,CTG | P,L 258 | XP_016857911.1 | |
XM_017002423.1 | 1355 | Intron | XP_016857912.1 |