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CGTGTCAATACTTTCCACATTTGTG[C/T]GTTTGAATGGATCCATGTGTTTAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600686 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
KPNA1 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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KPNA1 - karyopherin subunit alpha 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002264.3 | 6502 | UTR 3 | NP_002255.3 | |||
XM_005247437.3 | 6502 | Intron | XP_005247494.1 | |||
XM_005247439.3 | 6502 | Intron | XP_005247496.1 | |||
XM_011512795.2 | 6502 | Intron | XP_011511097.1 | |||
XM_011512797.2 | 6502 | Intron | XP_011511099.1 | |||
XM_017006363.1 | 6502 | Intron | XP_016861852.1 | |||
XM_017006364.1 | 6502 | Intron | XP_016861853.1 | |||
XM_017006365.1 | 6502 | Intron | XP_016861854.1 |
LOC102723582 - uncharacterized LOC102723582 | ||||||
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There are no transcripts associated with this gene. |
WDR5B - WD repeat domain 5B | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |