Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCTGTACTGGTCTGGAGCTGCACA[A/T]TCTTTTCAGACAACTCTTGTTCCAG
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 | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
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 | 3416 | Missense Mutation | AAT,ATT | N,I 936 | NP_001258856.1 | |
NM_001271928.1 | 3416 | Missense Mutation | AAT,ATT | N,I 905 | NP_001258857.1 | |
NM_017576.2 | 3416 | Missense Mutation | AAT,ATT | N,I 1002 | NP_060046.1 | |
XM_011518848.2 | 3416 | Missense Mutation | AAT,ATT | N,I 1028 | XP_011517150.1 | |
XM_011518849.2 | 3416 | Missense Mutation | AAT,ATT | N,I 1028 | XP_011517151.1 | |
XM_011518850.2 | 3416 | Missense Mutation | AAT,ATT | N,I 1028 | XP_011517152.1 | |
XM_011518854.2 | 3416 | Intron | XP_011517156.1 | |||
XM_011518856.2 | 3416 | Missense Mutation | AAT,ATT | N,I 1028 | XP_011517158.1 | |
XM_011518857.2 | 3416 | Missense Mutation | AAT,ATT | N,I 670 | XP_011517159.1 | |
XM_011518858.2 | 3416 | Missense Mutation | AAT,ATT | N,I 548 | XP_011517160.1 | |
XM_017014900.1 | 3416 | Missense Mutation | AAT,ATT | N,I 1028 | XP_016870389.1 | |
XM_017014901.1 | 3416 | Missense Mutation | AAT,ATT | N,I 1028 | XP_016870390.1 | |
XM_017014902.1 | 3416 | Missense Mutation | AAT,ATT | N,I 1028 | XP_016870391.1 | |
XM_017014903.1 | 3416 | Missense Mutation | AAT,ATT | N,I 1002 | XP_016870392.1 | |
XM_017014904.1 | 3416 | Missense Mutation | AAT,ATT | N,I 1002 | XP_016870393.1 | |
XM_017014905.1 | 3416 | Missense Mutation | AAT,ATT | N,I 962 | XP_016870394.1 | |
XM_017014906.1 | 3416 | Intron | XP_016870395.1 | |||
XM_017014907.1 | 3416 | Missense Mutation | AAT,ATT | N,I 936 | XP_016870396.1 | |
XM_017014908.1 | 3416 | Missense Mutation | AAT,ATT | N,I 905 | XP_016870397.1 | |
XM_017014909.1 | 3416 | Missense Mutation | AAT,ATT | N,I 876 | XP_016870398.1 | |
XM_017014910.1 | 3416 | Intron | XP_016870399.1 | |||
XM_017014911.1 | 3416 | Missense Mutation | AAT,ATT | N,I 644 | XP_016870400.1 | |
XM_017014912.1 | 3416 | Missense Mutation | AAT,ATT | N,I 522 | XP_016870401.1 | |
XM_017014913.1 | 3416 | Missense Mutation | AAT,ATT | N,I 522 | XP_016870402.1 | |
XM_017014914.1 | 3416 | Intron | XP_016870403.1 | |||
XM_017014915.1 | 3416 | Intron | XP_016870404.1 | |||
XM_017014916.1 | 3416 | Missense Mutation | AAT,ATT | N,I 393 | XP_016870405.1 |