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GCGCGAGACGCTGGACAGCGACGGT[A/G]TGGACGCGGCCGCGCTGGCCGAGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
EXOC3L4 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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EXOC3L4 - exocyst complex component 3 like 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077594.1 | 1099 | Missense Mutation | ATG,GTG | M,V 206 | NP_001071062.1 | |
XM_011537323.2 | 1099 | Missense Mutation | ATG,GTG | M,V 264 | XP_011535625.1 | |
XM_011537324.2 | 1099 | Missense Mutation | ATG,GTG | M,V 264 | XP_011535626.1 | |
XM_011537325.2 | 1099 | Missense Mutation | ATG,GTG | M,V 206 | XP_011535627.1 | |
XM_011537327.2 | 1099 | Missense Mutation | ATG,GTG | M,V 206 | XP_011535629.1 | |
XM_011537328.2 | 1099 | Missense Mutation | ATG,GTG | M,V 206 | XP_011535630.1 | |
XM_011537329.2 | 1099 | Missense Mutation | ATG,GTG | M,V 206 | XP_011535631.1 | |
XM_011537330.2 | 1099 | Missense Mutation | ATG,GTG | M,V 206 | XP_011535632.1 | |
XM_011537331.1 | 1099 | Missense Mutation | ATG,GTG | M,V 206 | XP_011535633.1 | |
XM_011537332.2 | 1099 | Missense Mutation | ATG,GTG | M,V 206 | XP_011535634.1 | |
XM_011537333.2 | 1099 | Missense Mutation | ATG,GTG | M,V 243 | XP_011535635.1 | |
XM_011537334.1 | 1099 | Missense Mutation | ATG,GTG | M,V 27 | XP_011535636.1 |