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GCAGCAGGAAAGAGCCCAATGCCCA[C/T]CGCAAGGATGGCACAAGGCTGGGCC
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 606 | Silent Mutation | CAC,CAT | H,H 41 | NP_001071062.1 | |
XM_011537323.2 | 606 | Silent Mutation | CAC,CAT | H,H 99 | XP_011535625.1 | |
XM_011537324.2 | 606 | Silent Mutation | CAC,CAT | H,H 99 | XP_011535626.1 | |
XM_011537325.2 | 606 | Silent Mutation | CAC,CAT | H,H 41 | XP_011535627.1 | |
XM_011537327.2 | 606 | Silent Mutation | CAC,CAT | H,H 41 | XP_011535629.1 | |
XM_011537328.2 | 606 | Silent Mutation | CAC,CAT | H,H 41 | XP_011535630.1 | |
XM_011537329.2 | 606 | Silent Mutation | CAC,CAT | H,H 41 | XP_011535631.1 | |
XM_011537330.2 | 606 | Silent Mutation | CAC,CAT | H,H 41 | XP_011535632.1 | |
XM_011537331.1 | 606 | Silent Mutation | CAC,CAT | H,H 41 | XP_011535633.1 | |
XM_011537332.2 | 606 | Silent Mutation | CAC,CAT | H,H 41 | XP_011535634.1 | |
XM_011537333.2 | 606 | Silent Mutation | CAC,CAT | H,H 78 | XP_011535635.1 | |
XM_011537334.1 | 606 | Intron | XP_011535636.1 |