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CCATCACCCCTGGCTCTACCCCGTC[A/C]CGTGGCTGCTGTAGTCAAAGACTCC
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 | |||
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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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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 | 3975 | Missense Mutation | GGG,GTG | G,V 1264 | NP_001186794.1 | |
NM_001199866.1 | 3975 | Intron | NP_001186795.1 | |||
NM_024704.4 | 3975 | Missense Mutation | GGG,GTG | G,V 1315 | NP_078980.3 | |
XM_005260750.3 | 3975 | Intron | XP_005260807.1 | |||
XM_005260751.4 | 3975 | Intron | XP_005260808.1 | |||
XM_005260752.3 | 3975 | Intron | XP_005260809.1 | |||
XM_005260753.3 | 3975 | Missense Mutation | GGG,GTG | G,V 1326 | XP_005260810.1 | |
XM_005260754.3 | 3975 | Missense Mutation | GGG,GTG | G,V 1296 | XP_005260811.1 | |
XM_005260755.3 | 3975 | Missense Mutation | GGG,GTG | G,V 1275 | XP_005260812.1 | |
XM_006723588.3 | 3975 | Missense Mutation | GGG,GTG | G,V 1285 | XP_006723651.1 | |
XM_017027926.1 | 3975 | Missense Mutation | GGG,GTG | G,V 1274 | XP_016883415.1 |