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TTGGGCACTTGGCAGAGCCAGGGCT[A/G]CATGGGGGTGCCCAGGGTGGGGGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611278 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KIF12 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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KIF12 - kinesin family member 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_138424.1 | 1730 | Silent Mutation | TGC,TGT | C,C 417 | NP_612433.1 | |
XM_005251683.4 | 1730 | Silent Mutation | TGC,TGT | C,C 555 | XP_005251740.1 | |
XM_006716947.2 | 1730 | Silent Mutation | TGC,TGT | C,C 521 | XP_006717010.1 | |
XM_011518190.2 | 1730 | Silent Mutation | TGC,TGT | C,C 613 | XP_011516492.1 | |
XM_011518191.2 | 1730 | Silent Mutation | TGC,TGT | C,C 613 | XP_011516493.1 | |
XM_011518192.2 | 1730 | UTR 3 | XP_011516494.1 | |||
XM_011518193.2 | 1730 | Intron | XP_011516495.1 | |||
XM_017014240.1 | 1730 | Silent Mutation | TGC,TGT | C,C 290 | XP_016869729.1 |