Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGCATTCCTCTGAGCTCACTGCTG[C/G]GGATGAGCCATGGAGCTCATAGACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
54 submissions
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Phenotype: |
MIM: 611279 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
KIF14 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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KIF14 - kinesin family member 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001305792.1 | 4648 | Missense Mutation | CCA,GCA | P,A 1142 | NP_001292721.1 | |
NM_014875.2 | 4648 | Missense Mutation | CCA,GCA | P,A 1633 | NP_055690.1 | |
XM_011510231.2 | 4648 | Missense Mutation | CCA,GCA | P,A 1633 | XP_011508533.1 | |
XM_011510232.2 | 4648 | Missense Mutation | CCA,GCA | P,A 1633 | XP_011508534.1 | |
XM_011510233.2 | 4648 | Missense Mutation | CCA,GCA | P,A 1605 | XP_011508535.1 | |
XM_011510235.2 | 4648 | Missense Mutation | CCA,GCA | P,A 1509 | XP_011508537.1 | |
XM_011510236.1 | 4648 | Missense Mutation | CCA,GCA | P,A 1142 | XP_011508538.1 | |
XM_017003005.1 | 4648 | Missense Mutation | CCA,GCA | P,A 1633 | XP_016858494.1 | |
XM_017003006.1 | 4648 | Missense Mutation | CCA,GCA | P,A 1590 | XP_016858495.1 | |
XM_017003007.1 | 4648 | Missense Mutation | CCA,GCA | P,A 1444 | XP_016858496.1 |
Set Membership: |
HapMap Validated |