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TAGAACGTGATCGTGTTCTTGACCT[C/T]GATCGACTTGCACTTCTGCTATTTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613384 | ||||||||||||||||||||
Literature Links: |
CCNL1 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 |
CCNL1 - cyclin L1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308185.1 | 1322 | Silent Mutation | TCA,TCG | S,S 395 | NP_001295114.1 | |
NM_020307.3 | 1322 | Silent Mutation | TCA,TCG | S,S 395 | NP_064703.1 | |
XM_005247648.3 | 1322 | Silent Mutation | TCA,TCG | S,S 240 | XP_005247705.1 | |
XM_006713710.3 | 1322 | Intron | XP_006713773.1 | |||
XM_011513011.2 | 1322 | Silent Mutation | TCA,TCG | S,S 240 | XP_011511313.1 | |
XM_017006891.1 | 1322 | Silent Mutation | TCA,TCG | S,S 189 | XP_016862380.1 | |
XM_017006892.1 | 1322 | Silent Mutation | TCA,TCG | S,S 168 | XP_016862381.1 | |
XM_017006893.1 | 1322 | Silent Mutation | TCA,TCG | S,S 168 | XP_016862382.1 | |
XM_017006894.1 | 1322 | Silent Mutation | TCA,TCG | S,S 168 | XP_016862383.1 | |
XM_017006895.1 | 1322 | Silent Mutation | TCA,TCG | S,S 168 | XP_016862384.1 | |
XM_017006896.1 | 1322 | Silent Mutation | TCA,TCG | S,S 168 | XP_016862385.1 | |
XM_017006897.1 | 1322 | Intron | XP_016862386.1 |