Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608283 | |||||||||||||||||||||||||||||
Literature Links: |
KIF21A PubMed Links | |||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
KIF21A - kinesin family member 21A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001173463.1 | 5225 | Missense Mutation | GAT,GGT | D,G 1587 | NP_001166934.1 | |
NM_001173464.1 | 5225 | Missense Mutation | GAT,GGT | D,G 1624 | NP_001166935.1 | |
NM_001173465.1 | 5225 | Missense Mutation | GAT,GGT | D,G 1571 | NP_001166936.1 | |
NM_017641.3 | 5225 | Missense Mutation | GAT,GGT | D,G 1611 | NP_060111.2 | |
XM_005269007.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1625 | XP_005269064.1 | |
XM_005269008.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1620 | XP_005269065.1 | |
XM_005269009.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1618 | XP_005269066.1 | |
XM_005269010.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1612 | XP_005269067.1 | |
XM_005269011.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1607 | XP_005269068.1 | |
XM_005269012.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1582 | XP_005269069.1 | |
XM_005269013.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1577 | XP_005269070.1 | |
XM_005269014.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1564 | XP_005269071.1 | |
XM_006719493.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1605 | XP_006719556.1 | |
XM_006719494.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1581 | XP_006719557.1 | |
XM_011538556.2 | 5225 | Missense Mutation | GAT,GGT | D,G 1602 | XP_011536858.1 | |
XM_017019607.1 | 5225 | Missense Mutation | GAT,GGT | D,G 1607 | XP_016875096.1 | |
XM_017019608.1 | 5225 | Missense Mutation | GAT,GGT | D,G 1594 | XP_016875097.1 | |
XM_017019609.1 | 5225 | Missense Mutation | GAT,GGT | D,G 1557 | XP_016875098.1 | |
XM_017019610.1 | 5225 | Missense Mutation | GAT,GGT | D,G 1557 | XP_016875099.1 | |
XM_017019611.1 | 5225 | Missense Mutation | GAT,GGT | D,G 1551 | XP_016875100.1 |
Set Membership: |
HapMap |