Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCATCCTGCTTGCCGCTGCTGCTGA[C/A]GCTGCTGTCACACTGCGTGTCCAGG
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 |
---|---|---|
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 |
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 | 2371 | Intron | NP_001155179.1 | |||
NM_001301097.1 | 2371 | Missense Mutation | NP_001288026.1 | |||
NM_032531.3 | 2371 | Missense Mutation | NP_115920.1 | |||
XM_011543026.2 | 2371 | Missense Mutation | XP_011541328.1 | |||
XM_011543027.2 | 2371 | Missense Mutation | XP_011541329.1 | |||
XM_011543028.2 | 2371 | Missense Mutation | XP_011541330.1 | |||
XM_011543030.2 | 2371 | Missense Mutation | XP_011541332.1 | |||
XM_011543031.2 | 2371 | Missense Mutation | XP_011541333.1 | |||
XM_011543032.2 | 2371 | Missense Mutation | XP_011541334.1 | |||
XM_011543033.1 | 2371 | Missense Mutation | XP_011541335.1 | |||
XM_017018418.1 | 2371 | Missense Mutation | XP_016873907.1 | |||
XM_017018419.1 | 2371 | Missense Mutation | XP_016873908.1 | |||
XM_017018420.1 | 2371 | Missense Mutation | 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 | 2371 | Intron | NP_001241686.1 | |||
NM_001254758.1 | 2371 | Intron | NP_001241687.1 | |||
NM_001254759.1 | 2371 | Intron | NP_001241688.1 | |||
NM_006278.2 | 2371 | Intron | NP_006269.1 | |||
XM_011542959.1 | 2371 | Intron | XP_011541261.1 | |||
XM_011542960.2 | 2371 | Intron | XP_011541262.1 | |||
XM_017018134.1 | 2371 | Intron | XP_016873623.1 |