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Search Thermo Fisher Scientific
ATGTTGCGGACTGGAGCATCACGCT[G/T]AAAAAGTCCCTGAGGTATTTCTGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
KIF16B 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 |
KIF16B - kinesin family member 16B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199865.1 | 3847 | Missense Mutation | TTA,TTC | L,F 1221 | NP_001186794.1 | |
NM_001199866.1 | 3847 | Intron | NP_001186795.1 | |||
NM_024704.4 | 3847 | Missense Mutation | TTA,TTC | L,F 1272 | NP_078980.3 | |
XM_005260750.3 | 3847 | Intron | XP_005260807.1 | |||
XM_005260751.4 | 3847 | Intron | XP_005260808.1 | |||
XM_005260752.3 | 3847 | Intron | XP_005260809.1 | |||
XM_005260753.3 | 3847 | Missense Mutation | TTA,TTC | L,F 1283 | XP_005260810.1 | |
XM_005260754.3 | 3847 | Missense Mutation | TTA,TTC | L,F 1253 | XP_005260811.1 | |
XM_005260755.3 | 3847 | Missense Mutation | TTA,TTC | L,F 1232 | XP_005260812.1 | |
XM_006723588.3 | 3847 | Missense Mutation | TTA,TTC | L,F 1242 | XP_006723651.1 | |
XM_017027926.1 | 3847 | Missense Mutation | TTA,TTC | L,F 1231 | XP_016883415.1 |