Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAATGCAGGGCAACCACGCAACAG[C/G]CCCTGAGCAAGGCCCCGATGTTATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605772 MIM: 611568 | ||||||||||||||||||||
Literature Links: |
EBAG9 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 |
EBAG9 - estrogen receptor binding site associated, antigen, 9 | ||||||
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There are no transcripts associated with this gene. |
SYBU - syntabulin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099743.1 | 2204 | Missense Mutation | GCC,GGC | A,G 644 | NP_001093213.1 | |
NM_001099744.1 | 2204 | Missense Mutation | GCC,GGC | A,G 645 | NP_001093214.1 | |
NM_001099745.1 | 2204 | Missense Mutation | GCC,GGC | A,G 645 | NP_001093215.1 | |
NM_001099746.1 | 2204 | Missense Mutation | GCC,GGC | A,G 526 | NP_001093216.1 | |
NM_001099747.1 | 2204 | Missense Mutation | GCC,GGC | A,G 644 | NP_001093217.1 | |
NM_001099748.1 | 2204 | Missense Mutation | GCC,GGC | A,G 645 | NP_001093218.1 | |
NM_001099749.1 | 2204 | Missense Mutation | GCC,GGC | A,G 526 | NP_001093219.1 | |
NM_001099750.1 | 2204 | Missense Mutation | GCC,GGC | A,G 645 | NP_001093220.1 | |
NM_001099751.1 | 2204 | Missense Mutation | GCC,GGC | A,G 644 | NP_001093221.1 | |
NM_001099752.1 | 2204 | Missense Mutation | GCC,GGC | A,G 645 | NP_001093222.1 | |
NM_001099753.1 | 2204 | Missense Mutation | GCC,GGC | A,G 644 | NP_001093223.1 | |
NM_001099754.1 | 2204 | Missense Mutation | GCC,GGC | A,G 645 | NP_001093224.1 | |
NM_001099755.1 | 2204 | Missense Mutation | GCC,GGC | A,G 526 | NP_001093225.1 | |
NM_001099756.1 | 2204 | Missense Mutation | GCC,GGC | A,G 642 | NP_001093226.1 | |
NM_017786.5 | 2204 | Missense Mutation | GCC,GGC | A,G 644 | NP_060256.3 | |
XM_005250999.1 | 2204 | Missense Mutation | GCC,GGC | A,G 515 | XP_005251056.1 | |
XM_005251000.1 | 2204 | Missense Mutation | GCC,GGC | A,G 482 | XP_005251057.1 | |
XM_011517154.2 | 2204 | Missense Mutation | GCC,GGC | A,G 478 | XP_011515456.1 | |
XM_017013614.1 | 2204 | Missense Mutation | GCC,GGC | A,G 526 | XP_016869103.1 | |
XM_017013615.1 | 2204 | Missense Mutation | GCC,GGC | A,G 526 | XP_016869104.1 |