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TGTACATCTCCTCGGAGCCTTCCTC[A/G]CTGTCGTTCTCCTCTGACTCGGTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608148 | ||||||||||||||||||||
Literature Links: |
SATB2 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 |
SATB2 - SATB homeobox 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172509.1 | 2522 | Silent Mutation | AGC,AGT | S,S 703 | NP_001165980.1 | |
NM_001172517.1 | 2522 | Silent Mutation | AGC,AGT | S,S 703 | NP_001165988.1 | |
NM_015265.3 | 2522 | Silent Mutation | AGC,AGT | S,S 703 | NP_056080.1 | |
XM_005246396.2 | 2522 | Silent Mutation | AGC,AGT | S,S 645 | XP_005246453.1 | |
XM_006712372.2 | 2522 | Silent Mutation | AGC,AGT | S,S 703 | XP_006712435.1 | |
XM_011510840.2 | 2522 | Silent Mutation | AGC,AGT | S,S 703 | XP_011509142.1 | |
XM_017003656.1 | 2522 | Silent Mutation | AGC,AGT | S,S 645 | XP_016859145.1 |