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GGGTAGCTGAGCCGGCTGCATAGGC[G/T]CAGTCTGTGATGGGGGAGTTCTGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613178 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CTIF 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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CTIF - cap binding complex dependent translation initiation factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142397.1 | Intron | NP_001135869.1 | ||||
NM_014772.2 | Intron | NP_055587.1 | ||||
XM_005258392.4 | Intron | XP_005258449.1 | ||||
XM_006722583.3 | Intron | XP_006722646.1 | ||||
XM_006722586.3 | Intron | XP_006722649.1 | ||||
XM_006722587.3 | Intron | XP_006722650.1 | ||||
XM_006722588.3 | Intron | XP_006722651.1 | ||||
XM_006722589.3 | Intron | XP_006722652.1 | ||||
XM_011526278.2 | Intron | XP_011524580.1 | ||||
XM_011526279.2 | Intron | XP_011524581.1 | ||||
XM_017026100.1 | Intron | XP_016881589.1 | ||||
XM_017026101.1 | Intron | XP_016881590.1 | ||||
XM_017026102.1 | Intron | XP_016881591.1 |