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ATAGGGGTGTGGATTAGAGGAGCTC[A/G]ATGGGCCTGCCTAGCTTAGAAATGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613919 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KIF6 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
|
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
|
KIF6 - kinesin family member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289020.1 | 2182 | UTR 3 | NP_001275949.1 | |||
NM_001289021.1 | 2182 | UTR 3 | NP_001275950.1 | |||
NM_001289024.1 | 2182 | UTR 3 | NP_001275953.1 | |||
NM_145027.4 | 2182 | UTR 3 | NP_659464.3 | |||
XM_005248904.4 | 2182 | Intron | XP_005248961.1 | |||
XM_011514357.2 | 2182 | Intron | XP_011512659.1 | |||
XM_011514358.2 | 2182 | Intron | XP_011512660.1 | |||
XM_011514359.2 | 2182 | Intron | XP_011512661.1 | |||
XM_011514361.2 | 2182 | Intron | XP_011512663.1 | |||
XM_017010427.1 | 2182 | Intron | XP_016865916.1 | |||
XM_017010428.1 | 2182 | Intron | XP_016865917.1 |