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CCAATAAGTTCCAGTAAGAGAAAAA[A/C]CAAAAAACAGCTCCCTTCTTGGAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
HDX 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 |
HDX - highly divergent homeobox | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001177478.1 | Intron | NP_001170949.1 | ||||
NM_001177479.1 | Intron | NP_001170950.1 | ||||
NM_144657.4 | Intron | NP_653258.2 | ||||
XM_006724619.1 | Intron | XP_006724682.1 | ||||
XM_011530863.2 | Intron | XP_011529165.1 | ||||
XM_011530864.1 | Intron | XP_011529166.1 | ||||
XM_017029274.1 | Intron | XP_016884763.1 | ||||
XM_017029275.1 | Intron | XP_016884764.1 |