Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611253 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
KIF27 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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KIF27 - kinesin family member 27 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271927.1 | 3597 | Silent Mutation | ATA,ATT | I,I 996 | NP_001258856.1 | |
NM_001271928.1 | 3597 | Silent Mutation | ATA,ATT | I,I 965 | NP_001258857.1 | |
NM_017576.2 | 3597 | Silent Mutation | ATA,ATT | I,I 1062 | NP_060046.1 | |
XM_011518848.2 | 3597 | Missense Mutation | ATA,ATT | I,I 1088 | XP_011517150.1 | |
XM_011518849.2 | 3597 | Missense Mutation | ATA,ATT | I,I 1088 | XP_011517151.1 | |
XM_011518850.2 | 3597 | Missense Mutation | ATA,ATT | I,I 1088 | XP_011517152.1 | |
XM_011518854.2 | 3597 | Missense Mutation | ATA,ATT | I,I 957 | XP_011517156.1 | |
XM_011518856.2 | 3597 | Missense Mutation | ATA,ATT | I,I 1088 | XP_011517158.1 | |
XM_011518857.2 | 3597 | Missense Mutation | ATA,ATT | I,I 730 | XP_011517159.1 | |
XM_011518858.2 | 3597 | Missense Mutation | ATA,ATT | I,I 608 | XP_011517160.1 | |
XM_017014900.1 | 3597 | Missense Mutation | ATA,ATT | I,I 1088 | XP_016870389.1 | |
XM_017014901.1 | 3597 | Missense Mutation | ATA,ATT | I,I 1088 | XP_016870390.1 | |
XM_017014902.1 | 3597 | Missense Mutation | ATA,ATT | I,I 1088 | XP_016870391.1 | |
XM_017014903.1 | 3597 | Missense Mutation | ATA,ATT | I,I 1062 | XP_016870392.1 | |
XM_017014904.1 | 3597 | Missense Mutation | ATA,ATT | I,I 1062 | XP_016870393.1 | |
XM_017014905.1 | 3597 | Missense Mutation | ATA,ATT | I,I 1022 | XP_016870394.1 | |
XM_017014906.1 | 3597 | Missense Mutation | ATA,ATT | I,I 1016 | XP_016870395.1 | |
XM_017014907.1 | 3597 | Missense Mutation | ATA,ATT | I,I 996 | XP_016870396.1 | |
XM_017014908.1 | 3597 | Missense Mutation | ATA,ATT | I,I 965 | XP_016870397.1 | |
XM_017014909.1 | 3597 | Missense Mutation | ATA,ATT | I,I 936 | XP_016870398.1 | |
XM_017014910.1 | 3597 | Missense Mutation | ATA,ATT | I,I 931 | XP_016870399.1 | |
XM_017014911.1 | 3597 | Missense Mutation | ATA,ATT | I,I 704 | XP_016870400.1 | |
XM_017014912.1 | 3597 | Missense Mutation | ATA,ATT | I,I 582 | XP_016870401.1 | |
XM_017014913.1 | 3597 | Missense Mutation | ATA,ATT | I,I 582 | XP_016870402.1 | |
XM_017014914.1 | 3597 | Intron | XP_016870403.1 | |||
XM_017014915.1 | 3597 | Missense Mutation | ATA,ATT | I,I 510 | XP_016870404.1 | |
XM_017014916.1 | 3597 | Missense Mutation | ATA,ATT | I,I 453 | XP_016870405.1 |
Set Membership: |
HapMap |