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ATGTCCTGGCTGAGATTCAGTCTTT[C/T]GAACTGCCTGTTGAAGCTACTTTAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609672 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EXOC6 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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EXOC6 - exocyst complex component 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001013848.3 | 261 | Silent Mutation | TTC,TTT | F,F 20 | NP_001013870.1 | |
NM_001319194.1 | 261 | Silent Mutation | TTC,TTT | F,F 41 | NP_001306123.1 | |
NM_001319195.1 | 261 | Intron | NP_001306124.1 | |||
NM_001319200.1 | 261 | Intron | NP_001306129.1 | |||
NM_019053.5 | 261 | Intron | NP_061926.3 | |||
XM_017016344.1 | 261 | Silent Mutation | TTC,TTT | F,F 41 | XP_016871833.1 | |
XM_017016345.1 | 261 | Silent Mutation | TTC,TTT | F,F 20 | XP_016871834.1 | |
XM_017016346.1 | 261 | Silent Mutation | TTC,TTT | F,F 20 | XP_016871835.1 | |
XM_017016347.1 | 261 | Intron | XP_016871836.1 | |||
XM_017016348.1 | 261 | Silent Mutation | TTC,TTT | F,F 41 | XP_016871837.1 |