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CATTCTCTAACTTGGAATGCAGCTG[A/G]CTGGGGTGGTGGAGCCCATCGGAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605433 | ||||||||||||||||||||
Literature Links: |
KIF13A 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 |
KIF13A - kinesin family member 13A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105566.2 | 5498 | Silent Mutation | AGC,AGT | S,S 1746 | NP_001099036.1 | |
NM_001105567.2 | 5498 | Silent Mutation | AGC,AGT | S,S 1733 | NP_001099037.1 | |
NM_001105568.2 | 5498 | Silent Mutation | AGC,AGT | S,S 1733 | NP_001099038.1 | |
NM_001243423.1 | 5498 | Intron | NP_001230352.1 | |||
NM_022113.5 | 5498 | Silent Mutation | AGC,AGT | S,S 1781 | NP_071396.4 | |
XM_011514806.2 | 5498 | Intron | XP_011513108.1 | |||
XM_017011188.1 | 5498 | Silent Mutation | AGC,AGT | S,S 1781 | XP_016866677.1 | |
XM_017011189.1 | 5498 | Silent Mutation | AGC,AGT | S,S 1768 | XP_016866678.1 | |
XM_017011190.1 | 5498 | Silent Mutation | AGC,AGT | S,S 1760 | XP_016866679.1 | |
XM_017011191.1 | 5498 | Silent Mutation | AGC,AGT | S,S 1747 | XP_016866680.1 | |
XM_017011192.1 | 5498 | Silent Mutation | AGC,AGT | S,S 1746 | XP_016866681.1 | |
XM_017011193.1 | 5498 | Silent Mutation | AGC,AGT | S,S 1670 | XP_016866682.1 |