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GATGGCTGGAATGGCAGAGGGACTC[A/G]TCAGGCGACCTGCAACCCCGAGCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609074 MIM: 603002 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBXW9 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FBXW9 - F-box and WD repeat domain containing 9 | ||||||
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There are no transcripts associated with this gene. |
SNORD135 - small nucleolar RNA, C/D box 135 | ||||||
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There are no transcripts associated with this gene. |
SNORD41 - small nucleolar RNA, C/D box 41 | ||||||
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There are no transcripts associated with this gene. |
TNPO2 - transportin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136195.1 | 2500 | Intron | NP_001129667.1 | |||
NM_001136196.1 | 2500 | Missense Mutation | ACG,ATG | T,M 772 | NP_001129668.1 | |
NM_013433.4 | 2500 | Intron | NP_038461.2 |