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GAAAGCATTTTCAAAGTCTTGATAT[A/G]TAACGGGCCTCAACTGGCTGGGCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605295 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FIGN 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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FIGN - fidgetin, microtubule severing factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321825.1 | 2489 | Missense Mutation | ACA,ATA | T,I 714 | NP_001308754.1 | |
NM_018086.3 | 2489 | Missense Mutation | ACA,ATA | T,I 725 | NP_060556.2 | |
XM_011511389.2 | 2489 | Missense Mutation | ACA,ATA | T,I 751 | XP_011509691.1 | |
XM_017004419.1 | 2489 | Missense Mutation | ACA,ATA | T,I 751 | XP_016859908.1 |