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AAAAGTGCCTACACATCAGTATTCA[A/C]ACCCACTGAATCCTACTGGGTGTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
8 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 |
---|---|---|
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 |
KIF14 - kinesin family member 14 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001305792.1 | 4695 | Silent Mutation | NP_001292721.1 | |||
NM_014875.2 | 4695 | Silent Mutation | NP_055690.1 | |||
XM_011510231.2 | 4695 | Silent Mutation | XP_011508533.1 | |||
XM_011510232.2 | 4695 | Silent Mutation | XP_011508534.1 | |||
XM_011510233.2 | 4695 | Silent Mutation | XP_011508535.1 | |||
XM_011510235.2 | 4695 | Silent Mutation | XP_011508537.1 | |||
XM_011510236.1 | 4695 | Silent Mutation | XP_011508538.1 | |||
XM_017003005.1 | 4695 | Silent Mutation | XP_016858494.1 | |||
XM_017003006.1 | 4695 | Silent Mutation | XP_016858495.1 | |||
XM_017003007.1 | 4695 | Silent Mutation | XP_016858496.1 |