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GGGGAGGAATGAAAGGTTCTGTCCC[A/G]AGCACAGAAATGTCAAGGAAGCTAT
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 | |||
---|---|---|---|---|---|
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
|
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 | Intron | NP_001166934.1 | ||||
NM_001173464.1 | Intron | NP_001166935.1 | ||||
NM_001173465.1 | Intron | NP_001166936.1 | ||||
NM_017641.3 | Intron | NP_060111.2 | ||||
XM_005269007.2 | Intron | XP_005269064.1 | ||||
XM_005269008.2 | Intron | XP_005269065.1 | ||||
XM_005269009.2 | Intron | XP_005269066.1 | ||||
XM_005269010.2 | Intron | XP_005269067.1 | ||||
XM_005269011.2 | Intron | XP_005269068.1 | ||||
XM_005269012.2 | Intron | XP_005269069.1 | ||||
XM_005269013.2 | Intron | XP_005269070.1 | ||||
XM_005269014.2 | Intron | XP_005269071.1 | ||||
XM_006719493.2 | Intron | XP_006719556.1 | ||||
XM_006719494.2 | Intron | XP_006719557.1 | ||||
XM_011538556.2 | Intron | XP_011536858.1 | ||||
XM_017019607.1 | Intron | XP_016875096.1 | ||||
XM_017019608.1 | Intron | XP_016875097.1 | ||||
XM_017019609.1 | Intron | XP_016875098.1 | ||||
XM_017019610.1 | Intron | XP_016875099.1 | ||||
XM_017019611.1 | Intron | XP_016875100.1 |