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GTGGTGGAGGAGCCACGGGCTGGTG[G/T]GCTGGGCACCAACGGGCACCCTCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612980 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IMP3 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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IMP3 - IMP3, U3 small nucleolar ribonucleoprotein | ||||||
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There are no transcripts associated with this gene. |
LOC107984799 - translation initiation factor IF-2-like | ||||||
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There are no transcripts associated with this gene. |
SNX33 - sorting nexin 33 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318146.1 | 497 | Missense Mutation | GGG,GTG | G,V 134 | NP_001305075.1 | |
NM_153271.1 | 497 | Missense Mutation | GGG,GTG | G,V 134 | NP_695003.1 |