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ATGCCTATTTATTTGTCACTAATAA[C/T]GACAAAGACCGAGAAGGGCATGGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
7 submissions
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Phenotype: |
MIM: 615283 MIM: 616086 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
EXOC8 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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EXOC8 - exocyst complex component 8 | ||||||
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There are no transcripts associated with this gene. |
SPRTN - SprT-like N-terminal domain | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010984.3 | 817 | Silent Mutation | AAC,AAT | N,N 123 | NP_001010984.1 | |
NM_001261462.2 | 817 | Intron | NP_001248391.1 | |||
NM_032018.6 | 817 | Silent Mutation | AAC,AAT | N,N 123 | NP_114407.3 | |
XM_006711818.2 | 817 | Intron | XP_006711881.1 | |||
XM_011544289.2 | 817 | Intron | XP_011542591.1 |