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GCTTTTTGGCACAACTGTCTTCAGT[A/C]GGAGGAGGTGGGGGAGGCGCTTCTT
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SATB2 - SATB homeobox 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172509.1 | 2231 | Silent Mutation | NP_001165980.1 | |||
NM_001172517.1 | 2231 | Silent Mutation | NP_001165988.1 | |||
NM_015265.3 | 2231 | Silent Mutation | NP_056080.1 | |||
XM_005246396.2 | 2231 | Silent Mutation | XP_005246453.1 | |||
XM_006712372.2 | 2231 | Silent Mutation | XP_006712435.1 | |||
XM_011510840.2 | 2231 | Silent Mutation | XP_011509142.1 | |||
XM_017003656.1 | 2231 | Silent Mutation | XP_016859145.1 |