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AACGGCGGAATATGGGCGGGAACCA[C/G]TCCCACAAGCCCCCCGTGTTTGACG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LOC107986255 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
LOC107986255 - translation initiation factor IF-2-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017008890.1 | 362 | Intron | XP_016864379.1 |
STK32B - serine/threonine kinase 32B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306082.1 | 362 | UTR 5 | NP_001293011.1 | |||
NM_018401.2 | 362 | Silent Mutation | CAC,CAG | H,Q 5 | NP_060871.1 | |
XM_005247982.3 | 362 | Intron | XP_005248039.1 | |||
XM_005247983.4 | 362 | Intron | XP_005248040.1 | |||
XM_011513497.1 | 362 | Missense Mutation | CAC,CAG | H,Q 5 | XP_011511799.1 | |
XM_011513501.2 | 362 | Intron | XP_011511803.1 | |||
XM_011513504.1 | 362 | Intron | XP_011511806.1 | |||
XM_017008374.1 | 362 | Intron | XP_016863863.1 | |||
XM_017008375.1 | 362 | Intron | XP_016863864.1 | |||
XM_017008376.1 | 362 | Intron | XP_016863865.1 | |||
XM_017008377.1 | 362 | Intron | XP_016863866.1 |