Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTGGGCGTTTTCATTCAGCTTTGC[A/G]CTTCAATCCAGGGATTTTTGCTTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604475 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EML6 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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EML6 - echinoderm microtubule associated protein like 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039753.2 | 800 | Intron | NP_001034842.2 | |||
XM_017004098.1 | 800 | Intron | XP_016859587.1 | |||
XM_017004099.1 | 800 | Intron | XP_016859588.1 | |||
XM_017004100.1 | 800 | Intron | XP_016859589.1 | |||
XM_017004101.1 | 800 | Intron | XP_016859590.1 | |||
XM_017004102.1 | 800 | Intron | XP_016859591.1 |
RTN4 - reticulon 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321859.1 | 800 | Missense Mutation | NP_001308788.1 | |||
NM_001321860.1 | 800 | Missense Mutation | NP_001308789.1 | |||
NM_001321861.1 | 800 | Missense Mutation | NP_001308790.1 | |||
NM_001321862.1 | 800 | Missense Mutation | NP_001308791.1 | |||
NM_001321863.1 | 800 | Missense Mutation | NP_001308792.1 | |||
NM_001321904.1 | 800 | Missense Mutation | NP_001308833.1 | |||
NM_007008.2 | 800 | Missense Mutation | NP_008939.1 | |||
NM_020532.4 | 800 | Missense Mutation | NP_065393.1 | |||
NM_153828.2 | 800 | Missense Mutation | NP_722550.1 | |||
NM_207520.1 | 800 | Missense Mutation | NP_997403.1 | |||
NM_207521.1 | 800 | Missense Mutation | NP_997404.1 | |||
XM_005264434.3 | 800 | Missense Mutation | XP_005264491.1 | |||
XM_017004518.1 | 800 | Missense Mutation | XP_016860007.1 | |||
XM_017004519.1 | 800 | Missense Mutation | XP_016860008.1 |