Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607761 MIM: 104240 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KIRREL3 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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KIRREL3 - kin of IRRE like 3 (Drosophila) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001161707.1 | 2175 | Intron | NP_001155179.1 | |||
NM_001301097.1 | 2175 | Silent Mutation | GGC,GGT | G,G 653 | NP_001288026.1 | |
NM_032531.3 | 2175 | Silent Mutation | GGC,GGT | G,G 665 | NP_115920.1 | |
XM_011543026.2 | 2175 | Silent Mutation | GGC,GGT | G,G 696 | XP_011541328.1 | |
XM_011543027.2 | 2175 | Silent Mutation | GGC,GGT | G,G 690 | XP_011541329.1 | |
XM_011543028.2 | 2175 | Silent Mutation | GGC,GGT | G,G 690 | XP_011541330.1 | |
XM_011543030.2 | 2175 | Silent Mutation | GGC,GGT | G,G 671 | XP_011541332.1 | |
XM_011543031.2 | 2175 | Silent Mutation | GGC,GGT | G,G 665 | XP_011541333.1 | |
XM_011543032.2 | 2175 | Silent Mutation | GGC,GGT | G,G 659 | XP_011541334.1 | |
XM_011543033.1 | 2175 | Silent Mutation | GGC,GGT | G,G 653 | XP_011541335.1 | |
XM_017018418.1 | 2175 | Silent Mutation | GGC,GGT | G,G 690 | XP_016873907.1 | |
XM_017018419.1 | 2175 | Silent Mutation | GGC,GGT | G,G 678 | XP_016873908.1 | |
XM_017018420.1 | 2175 | Silent Mutation | GGC,GGT | G,G 665 | XP_016873909.1 |
ST3GAL4 - ST3 beta-galactoside alpha-2,3-sialyltransferase 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001254757.1 | 2175 | Intron | NP_001241686.1 | |||
NM_001254758.1 | 2175 | Intron | NP_001241687.1 | |||
NM_001254759.1 | 2175 | Intron | NP_001241688.1 | |||
NM_006278.2 | 2175 | Intron | NP_006269.1 | |||
XM_011542959.1 | 2175 | Intron | XP_011541261.1 | |||
XM_011542960.2 | 2175 | Intron | XP_011541262.1 | |||
XM_017018134.1 | 2175 | Intron | XP_016873623.1 |