Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGCAGATGTGGCAGCAGGGGCAGG[G/A]GTAGAGGGGTGGCAGTGCCTGCAAA
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 |
---|---|---|
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 |
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 | 1575 | Missense Mutation | CCC,TCC | P,S 366 | NP_612433.1 | |
XM_005251683.4 | 1575 | Missense Mutation | CCC,TCC | P,S 504 | XP_005251740.1 | |
XM_006716947.2 | 1575 | Missense Mutation | CCC,TCC | P,S 470 | XP_006717010.1 | |
XM_011518190.2 | 1575 | Missense Mutation | CCC,TCC | P,S 562 | XP_011516492.1 | |
XM_011518191.2 | 1575 | Missense Mutation | CCC,TCC | P,S 562 | XP_011516493.1 | |
XM_011518192.2 | 1575 | Missense Mutation | CCC,TCC | P,S 562 | XP_011516494.1 | |
XM_011518193.2 | 1575 | Intron | XP_011516495.1 | |||
XM_017014240.1 | 1575 | Missense Mutation | CCC,TCC | P,S 239 | XP_016869729.1 |