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TCTCATTCTGCTTTGATTTCCTTTG[A/T]ACATATGACTTATAATCCCCATTAG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 604538 | |||||||||||||||||||||||
Literature Links: |
KIF2C PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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)
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EUR - Not Available | |||||
AMR - Not Available |
KIF2C - kinesin family member 2C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297655.1 | Intron | NP_001284584.1 | ||||
NM_001297656.1 | Intron | NP_001284585.1 | ||||
NM_001297657.1 | Intron | NP_001284586.1 | ||||
NM_006845.3 | Intron | NP_006836.2 | ||||
XM_011540540.2 | Intron | XP_011538842.1 | ||||
XM_011540541.2 | Intron | XP_011538843.1 |
Set Membership: |
HapMap |