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GCTCCCGTGACCTGCTTCGAGAACG[A/G]GAAGAACTCCGGCTCCGAGACTTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
CCNL2 - cyclin L2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039577.3 | 1317 | Intron | NP_001034666.1 | |||
NM_001320153.1 | 1317 | Silent Mutation | TCC,TCT | S,S 245 | NP_001307082.1 | |
NM_001320155.1 | 1317 | Silent Mutation | TCC,TCT | S,S 245 | NP_001307084.1 | |
NM_030937.4 | 1317 | Silent Mutation | TCC,TCT | S,S 467 | NP_112199.2 | |
XM_011542216.2 | 1317 | Silent Mutation | TCC,TCT | S,S 500 | XP_011540518.1 | |
XM_011542219.2 | 1317 | Silent Mutation | TCC,TCT | S,S 336 | XP_011540521.1 | |
XM_011542221.2 | 1317 | Silent Mutation | TCC,TCT | S,S 245 | XP_011540523.1 | |
XM_017002420.1 | 1317 | Silent Mutation | TCC,TCT | S,S 345 | XP_016857909.1 | |
XM_017002421.1 | 1317 | Silent Mutation | TCC,TCT | S,S 336 | XP_016857910.1 | |
XM_017002422.1 | 1317 | Silent Mutation | TCC,TCT | S,S 245 | XP_016857911.1 | |
XM_017002423.1 | 1317 | Intron | XP_016857912.1 |