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GTTGCGAATACTTTCAACACAAGTC[C/T]GGAGAAGATTTATATCACTATGGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
4 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 - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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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
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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 | 4346 | Missense Mutation | CAG,CGG | Q,R 1041 | NP_001292721.1 | |
NM_014875.2 | 4346 | Missense Mutation | CAG,CGG | Q,R 1532 | NP_055690.1 | |
XM_011510231.2 | 4346 | Missense Mutation | CAG,CGG | Q,R 1532 | XP_011508533.1 | |
XM_011510232.2 | 4346 | Missense Mutation | CAG,CGG | Q,R 1532 | XP_011508534.1 | |
XM_011510233.2 | 4346 | Missense Mutation | CAG,CGG | Q,R 1504 | XP_011508535.1 | |
XM_011510235.2 | 4346 | Missense Mutation | CAG,CGG | Q,R 1408 | XP_011508537.1 | |
XM_011510236.1 | 4346 | Missense Mutation | CAG,CGG | Q,R 1041 | XP_011508538.1 | |
XM_017003005.1 | 4346 | Missense Mutation | CAG,CGG | Q,R 1532 | XP_016858494.1 | |
XM_017003006.1 | 4346 | Missense Mutation | CAG,CGG | Q,R 1489 | XP_016858495.1 | |
XM_017003007.1 | 4346 | Missense Mutation | CAG,CGG | Q,R 1343 | XP_016858496.1 |