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CTGATGAGGTCCTTTCCATTCCTCC[C/G]GTTGCTAGGGCACAGGGGACTCAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614570 | ||||||||||||||||||||
Literature Links: |
KIF18B 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 |
KIF18B - kinesin family member 18B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001264573.1 | 2654 | UTR 3 | NP_001251503.1 | |||
NM_001265577.1 | 2654 | Missense Mutation | CGG,GGG | R,G 829 | NP_001252506.1 | |
XM_011524385.2 | 2654 | Missense Mutation | CGG,GGG | R,G 850 | XP_011522687.1 | |
XM_011524386.2 | 2654 | Missense Mutation | CGG,GGG | R,G 841 | XP_011522688.1 | |
XM_011524387.2 | 2654 | Missense Mutation | CGG,GGG | R,G 841 | XP_011522689.1 | |
XM_011524388.2 | 2654 | Missense Mutation | CGG,GGG | R,G 838 | XP_011522690.1 | |
XM_011524389.2 | 2654 | UTR 3 | XP_011522691.1 | |||
XM_011524390.2 | 2654 | Missense Mutation | CGG,GGG | R,G 815 | XP_011522692.1 | |
XM_011524391.2 | 2654 | Intron | XP_011522693.1 |
MIR6783 - microRNA 6783 | ||||||
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There are no transcripts associated with this gene. |