Product Details
- SNP ID
-
rs200035535
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:109574964 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGAATGCAGGGCAACCACGCAACAG[C/G]CCCTGAGCAAGGCCCCGATGTTATA
- Phenotype
-
MIM: 605772
MIM: 611568
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
EBAG9
PubMed Links
Gene Details
- Gene
- EBAG9
- Gene Name
- estrogen receptor binding site associated, antigen, 9
There are no transcripts associated with this gene.
- Gene
- SYBU
- Gene Name
- syntabulin
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001099743.1 |
2204 |
Missense Mutation |
GCC,GGC |
A644G |
NP_001093213.1 |
NM_001099744.1 |
2204 |
Missense Mutation |
GCC,GGC |
A645G |
NP_001093214.1 |
NM_001099745.1 |
2204 |
Missense Mutation |
GCC,GGC |
A645G |
NP_001093215.1 |
NM_001099746.1 |
2204 |
Missense Mutation |
GCC,GGC |
A526G |
NP_001093216.1 |
NM_001099747.1 |
2204 |
Missense Mutation |
GCC,GGC |
A644G |
NP_001093217.1 |
NM_001099748.1 |
2204 |
Missense Mutation |
GCC,GGC |
A645G |
NP_001093218.1 |
NM_001099749.1 |
2204 |
Missense Mutation |
GCC,GGC |
A526G |
NP_001093219.1 |
NM_001099750.1 |
2204 |
Missense Mutation |
GCC,GGC |
A645G |
NP_001093220.1 |
NM_001099751.1 |
2204 |
Missense Mutation |
GCC,GGC |
A644G |
NP_001093221.1 |
NM_001099752.1 |
2204 |
Missense Mutation |
GCC,GGC |
A645G |
NP_001093222.1 |
NM_001099753.1 |
2204 |
Missense Mutation |
GCC,GGC |
A644G |
NP_001093223.1 |
NM_001099754.1 |
2204 |
Missense Mutation |
GCC,GGC |
A645G |
NP_001093224.1 |
NM_001099755.1 |
2204 |
Missense Mutation |
GCC,GGC |
A526G |
NP_001093225.1 |
NM_001099756.1 |
2204 |
Missense Mutation |
GCC,GGC |
A642G |
NP_001093226.1 |
NM_017786.5 |
2204 |
Missense Mutation |
GCC,GGC |
A644G |
NP_060256.3 |
XM_005250999.1 |
2204 |
Missense Mutation |
GCC,GGC |
A515G |
XP_005251056.1 |
XM_005251000.1 |
2204 |
Missense Mutation |
GCC,GGC |
A482G |
XP_005251057.1 |
XM_011517154.2 |
2204 |
Missense Mutation |
GCC,GGC |
A478G |
XP_011515456.1 |
XM_017013614.1 |
2204 |
Missense Mutation |
GCC,GGC |
A526G |
XP_016869103.1 |
XM_017013615.1 |
2204 |
Missense Mutation |
GCC,GGC |
A526G |
XP_016869104.1 |
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