Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTTGATCTTTTTGCGAGACAGACAG[A/G]AGTCGGAGTCTGTCATATCATCTAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605802 | ||||||||||||||||||||
Literature Links: |
ZEB2 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 |
ZEB2 - zinc finger E-box binding homeobox 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001171653.1 | 3067 | Missense Mutation | TCC,TTC | S,F 960 | NP_001165124.1 | |
NM_014795.3 | 3067 | Missense Mutation | TCC,TTC | S,F 984 | NP_055610.1 | |
XM_006712881.3 | 3067 | Missense Mutation | TCC,TTC | S,F 984 | XP_006712944.1 | |
XM_006712882.3 | 3067 | Missense Mutation | TCC,TTC | S,F 984 | XP_006712945.1 | |
XM_011512232.2 | 3067 | Missense Mutation | TCC,TTC | S,F 977 | XP_011510534.1 | |
XM_017005414.1 | 3067 | Missense Mutation | TCC,TTC | S,F 872 | XP_016860903.1 | |
XM_017005415.1 | 3067 | Missense Mutation | TCC,TTC | S,F 872 | XP_016860904.1 |